Holley
Download as ppt, pdf0 likes432 views
This document defines muscular dystrophy as a progressive weakening of muscles as individual muscle fibers die and are replaced by connective tissue. It lists symptoms such as weakness in the hips and thighs. Long term effects include disability to walk by the teen years, abnormal bone development, and possible paralysis leading to death by the mid-20s. Current treatments aim to provide respiratory aid and physical therapy as there is no known cure.
1 of 7
Download to read offline
Ad
Recommended
Senior Project Research Paper
Senior Project Research PaperNicole T
油
The document discusses muscular dystrophy, a genetic disorder that causes muscles to weaken over time. It describes the different types of muscular dystrophy and their symptoms, such as loss of ability to walk or sit up. While there is no cure currently, organizations like the Muscular Dystrophy Association fund research through events like telethons in the hopes of finding effective treatments and a cure. The association aims to support those affected by the disease and further public understanding.All you need to learn about osteoporosis
All you need to learn about osteoporosisMedical and Health
油
Osteoporosis is a condition characterized by low bone mass and deterioration of bone tissue, leading to increased fragility and fractures, particularly in older adults and postmenopausal women. It can be classified as primary (type 1 and type 2) or secondary, with risk factors including age, gender, hormonal changes, and certain medications. Common fractures associated with osteoporosis occur in the hip, wrist, and spine, and preventive measures and treatments are available to manage the condition.Sub 2[1].2 FORM5
Sub 2[1].2 FORM5cikgushaik
油
The document discusses several consequences of an impaired musculoskeletal system, including muscle cramps, muscular dystrophy, osteoporosis, arthritis, and impaired mobility. Muscle cramps can last over 15 minutes and affect the hamstrings and calves. Muscular dystrophy is a genetic disorder that causes progressive muscle weakening and loss of strength. Osteoporosis causes bones to become hollow and brittle, increasing risk of fractures. Arthritis causes joint inflammation and cartilage breakdown, resulting in pain and stiffness. An impaired musculoskeletal system can limit one's ability to perform daily activities and move independently.Osteoporasis Disease Report
Osteoporasis Disease ReportBianca Butler
油
Osteoporosis is a disease where bones become weak and brittle, increasing the risk of fractures, especially in the hips, spine and wrists. It affects over 10 million Americans aged 50 and older, with women at higher risk than men. Risk factors include age, gender, family history and previous fractures. Symptoms may not appear until a fracture occurs. Treatment focuses on lifestyle changes like diet, exercise and medication to slow bone loss and reduce fracture risk. Complications can include pain, loss of mobility and independence from broken bones.Osteoporosis - Everything You Should Know
Osteoporosis - Everything You Should KnowPrathima Hospitals
油
Osteoporosis is a bone disorder characterized by low bone density, particularly affecting aging men and postmenopausal women, leading to increased fragility and fracture risk. It is associated with high morbidity and mortality, especially among older women, with significant under-diagnosis of related fractures. Management includes lifestyle modifications, calcium and vitamin D supplementation, and pharmacological therapies like bisphosphonates and hormone replacement therapy.Osteoporosis & it's Prevalence
Osteoporosis & it's PrevalenceMd.Reyashat Azim [Abir]
油
Osteoporosis is a chronic skeletal disorder characterized by excessive bone loss, leading to increased fracture risk and significant health consequences. The prevalence of osteoporosis is notable, with 1 in 3 women and 1 in 8 men over 50 years affected, and it results in serious complications such as fractures, decreased quality of life, and increased morbidity and mortality. Key warning signs include persistent back pain and spinal deformities, often making it asymptomatic until a fracture occurs.Osteoporosis- Prevention and Management
Osteoporosis- Prevention and ManagementPrathima Hospitals
油
Osteoporosis is a bone disorder characterized by low density and deterioration of bone architecture, leading to increased fracture risk, particularly in aging women and men. It results in millions of fractures annually, causing significant morbidity and mortality, especially among the elderly. Diagnosis involves assessing bone mineral density, and prevention includes lifestyle changes and, when necessary, pharmacological treatments to manage the risk and impact of the disease.Osteoporosis of Bones By Dr. Prakash Khalap
Osteoporosis of Bones By Dr. Prakash KhalapHealth Education Library for People
油
Osteoporosis is a metabolic bone disease characterized by low bone mass and increased fragility, leading to a higher risk of fractures. It predominantly affects urban populations, particularly older adults, women, and those with vitamin D deficiencies. Recommended treatments include a calcium-rich diet, vitamin D supplementation, weight-bearing exercises, and medications such as bisphosphonates.Autism
AutismMr. Holley's H.I. Classes
油
Autism is a disorder marked by problems with social interaction and communication, as well as restrictive and repetitive behaviors. Some people are born with autism while others develop it later in life. Symptoms typically emerge between ages 2-3 and may include lack of social engagement, delayed language development, and stimming behaviors like hand flapping. While there is no cure, early intervention through specialized education programs can help children with autism improve their communication and learning skills. Providing support is important, as autism often co-occurs with conditions like intellectual disabilities, seizures, or genetic syndromes.Cerebral palsy
Cerebral palsyMr. Holley's H.I. Classes
油
Cerebral palsy is a motor disability caused by abnormal brain development before one month of age that results in a lack of normal movement control. Symptoms may not appear until 9-24 months as the brain areas controlling movement are immature. There is no cure, but physical, occupational, and behavioral therapies can help improve motor skills and independence as well as prevent deformities through medications, braces, and sometimes surgery.Down syndrome
Down syndromeArie Dewi M Arif's
油
Down syndrome is a genetic disorder caused by a full or partial extra copy of chromosome 21. This additional genetic material alters development and causes characteristic physical traits like low muscle tone, small stature, and a single deep crease in the palm. Early intervention through therapies can help children with Down syndrome achieve basic skills and lay a foundation for future progress, as delays are common in areas like physical, cognitive, language, and social development. Education requires careful consideration and supports, though with interventions people with Down syndrome can learn at their own pace and have varied goals and roles.Spina bifida
Spina bifidaMr. Holley's H.I. Classes
油
Spina bifida is a birth defect that results from a mistake early in the development of the spinal cord. It causes symptoms like a bulging spinal cord, hydrocephalus, paralysis in the lower back and legs, and bladder and bowel issues. Spina bifida is a chronic condition meaning it cannot be cured, only treated, through surgery, medication, and physiotherapy. Many people with spina bifida will require assistive devices like braces, crutches, or wheelchairs.Spina bifida
Spina bifidaMr. Holley's H.I. Classes
油
Spina bifida is a birth defect that results from a mistake early in the development of the spinal cord, causing difficulties with feeding, breathing, swallowing, and arm stiffness. There is no known cure for nerve damage from spina bifida, but pediatric neurosurgeons can operate to close openings on the back to prevent further damage and infection. Volunteering at organizations that help people with spina bifida is one way to provide assistance.Down syndrome
Down syndromeMr. Holley's H.I. Classes
油
Down syndrome is a genetic condition that affects mental and physical development. People with Down syndrome may have some recognizable physical features but symptoms vary in severity. Common symptoms include delayed mental development, lack of muscle tone, and a flattened face. Individuals with Down syndrome also have an increased risk of health issues like leukemia, lung infections, Alzheimer's disease, and diabetes. While there is no cure for Down syndrome, educational and physical therapies can help. Genetic counseling may help assess risks for expectant mothers.Muscular dystrophy
Muscular dystrophyMr. Holley's H.I. Classes
油
Muscular dystrophy is a group of genetic diseases that progressively weaken muscles without a known cure. Symptoms vary depending on the type but can include muscle weakness, drooping eyelids, difficulty walking, and problems breathing in later stages. Treatment focuses on maintaining range of motion through passive stretching conducted by physical therapists and trained caregivers.Muscular dystrophy presentation
Muscular dystrophy presentationkkbauer
油
Muscular dystrophy is a group of inherited diseases that cause the voluntary muscles to progressively weaken over time. There are nine main types of muscular dystrophy that can affect any age or gender. Symptoms include muscle weakness, spasms, and difficulty with mobility. While there is no cure, treatment aims to relieve symptoms and slow progression through medications, therapy, exercise, and assistive devices. Researchers are working to develop new treatments like gene therapy.Hi power point
Hi power pointMr. Holley's H.I. Classes
油
Muscular dystrophy is a hereditary disease characterized by the gradual wasting of muscles. It sometimes also affects the heart. The symptoms include difficulty using muscle groups, drooping eyelids, frequent falls, and loss of muscle strength and size. Living with muscular dystrophy can make walking difficult and require the use of a wheelchair. It may also necessitate lifelong assistance with daily tasks like feeding. To help those affected, people can volunteer at disability homes by assisting with activities and providing support.Muscular Dystrophy Research Paper
Muscular Dystrophy Research PaperCwintzell1993
油
Muscular dystrophy is a genetic disorder that causes progressive muscle weakness. It is characterized by defects in muscle proteins and affects skeletal, heart and smooth muscles. The main symptoms are muscle weakness and deterioration over time, leading to difficulties with movement. There are many types of muscular dystrophy but they all involve degeneration of muscle fibers. Currently there is no cure, but treatment focuses on managing symptoms and slowing disease progression through exercise, physical therapy and other means. Researchers are working on developing new treatments such as gene therapy.Senior Project Research paper
Senior Project Research paperCwintzell1993
油
Muscular dystrophy is a genetic disorder that causes progressive muscle weakness. It is characterized by defects in muscle proteins and affects skeletal, heart and smooth muscles. The main symptoms are muscle weakness and deterioration over time, leading to difficulties with movement. There are many types of muscular dystrophy but they all involve degeneration of muscle fibers. Currently there is no cure, but treatment focuses on managing symptoms and slowing disease progression through exercise, physical therapy and other means. Researchers are working on developing new treatments such as gene therapy.Gene therapy for muscular dystrophy
Gene therapy for muscular dystrophyMohamed Elasaly, PT, CKTP, MSc Biotech.
油
The document discusses muscular dystrophy, focusing on its historical accounts, symptoms, and gene therapy approaches for treatment. It details the significance of the dystrophin gene and its role in muscular dystrophies, particularly Duchenne and Becker muscular dystrophy. Additionally, various gene therapy strategies, including gene augmentation, genome editing, and exon skipping, are explored as potential treatments for the condition.Muscular (autosaved) orignal
Muscular (autosaved) orignalNandkishor Rautrai
油
Muscular dystrophy is a group of muscle diseases that weaken the musculoskeletal system and hamper movement. There is currently no cure, but physiotherapy, exercise, supplements and medications can help maintain muscle strength. Researchers are investigating recombinant DNA therapies to restore dystrophin production. The document reviews the history, causes, symptoms, types, diagnosis and treatment of muscular dystrophy. Treatment options discussed include medications, physical therapy, surgery and assistive devices.Muscular Dystrophy!!
Muscular Dystrophy!!Jennifer Chora
油
Muscular dystrophy is a genetic disorder that causes muscles to weaken over time due to missing or defective genes preventing the body from producing necessary proteins. There are several types of muscular dystrophy affecting different muscle groups with varying degrees of severity. While there is no cure, treatment aims to preserve muscle and joint function and slow deterioration through therapies, braces, wheelchairs and respiratory support.DUCHENNE MUSCULAR DYSTROPHY
DUCHENNE MUSCULAR DYSTROPHYAniedu Ifeanyichukwu
油
Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle weakness. It is caused by an absence of the protein dystrophin due to mutations in the dystrophin gene on the X chromosome. The disease mainly affects boys and results in the breakdown of skeletal muscles. While there is no cure, treatment aims to manage symptoms and improve quality of life through physical therapy, bracing, medication, and respiratory/nutritional support. Research continues on new therapies such as gene therapy to replace the missing dystrophin protein.Muscular dystrophy
Muscular dystrophyCourtney
油
Muscular dystrophy (MD) is a genetic disease characterized by progressive muscle weakness and degeneration. There are over 30 types of MD that vary in age of onset, progression rate, and pattern of inheritance. The most common forms are Duchenne MD, which affects boys and leads to loss of mobility by age 20, and Becker's MD, which has a slower progression in males. Teachers can support students with MD by making accommodations, encouraging independence and peer interaction, and recommending counseling to help manage the physical and psychological impacts of the disease.mygeneticspresentation-141130173403-conversion-gate02.pptx
mygeneticspresentation-141130173403-conversion-gate02.pptxAnnaKhurshid
油
This document provides an overview of Duchenne muscular dystrophy (DMD). It begins with a brief history of the disease and its discovery. It then discusses the genetic basis and pathophysiology of DMD, which involves a mutation in the dystrophin gene. The clinical features and stages of DMD are outlined, from early ambulatory difficulties in childhood to loss of ambulation and eventual death often by the 30s due to respiratory or cardiac failure. Current treatment focuses on symptom management through physical therapy, bracing, medications, and nutritional support, though stem cell therapy and gene therapy show promise.Muscular Dustropy
Muscular Dustropytamscott5
油
Muscular Dystrophy is a genetic disorder that causes muscle weakness and wasting. It refers to a group of genetic disorders that destroy muscles over time. The most common type is Duchenne Muscular Dystrophy, which affects boys starting between ages 2-6 and causes progressive muscle degeneration and weakness. Eventually, people with DMD may need wheelchairs and ventilators and usually do not survive past their late teens or early adulthood due to heart and respiratory failure. While there is no cure for MD, research is ongoing to help manage symptoms and prolong life.MUSCULAR DYSTROPHY syndrome in child.pptx
MUSCULAR DYSTROPHY syndrome in child.pptxNarayanNeupane3
油
Muscular dystrophy is a group of genetic diseases that causes the muscles to weaken over time. The main symptom is progressive muscle weakness. There are many forms of muscular dystrophy that vary in their severity, affected muscles, age of onset, and progression. While there is no cure, treatment focuses on managing symptoms, slowing disease progression, and maintaining mobility and independence through medications, physical therapy, braces, and other assistive devices.Muscular dystrophy hi
Muscular dystrophy hiMr. Holley's H.I. Classes
油
Muscular dystrophy is a hereditary, progressive, and non-curable disease that causes the degeneration and weakness of skeletal muscles due to defective genes. There are several types of muscular dystrophy including Duchenne and Becker muscular dystrophy, which primarily affects males and can be life-threatening before age 20; limb-girdle dystrophy, which affects both genders and starts in the pelvis and legs; and facioscapulohumeral dystrophy, which relates to muscles in the face, shoulders, and arms. While there is no cure, treatment focuses on physical therapy, exercises, braces, and corrective surgery to relieve symptoms.Presentation2
Presentation2Mr. Holley's H.I. Classes
油
Muscular dystrophy is a genetic disorder that causes progressive muscle weakness and wasting. It is characterized by problems with coordination, mobility, muscle weakness, and joint stiffness. Over time, it can lead to an increased reliance on wheelchairs, crutches, or other mobility assistance as well as potential impacts to breathing and heart function. The specific type and severity of muscular dystrophy depends on the gene defects involved and at what age symptoms first appear.Duchenne Muscular Dystrophy
Duchenne Muscular DystrophyMyzak
油
Duchenne Muscular Dystrophy is a disease that causes rapidly worsening muscle weakness due to a lack of the protein dystrophin. It is inherited through an X-linked recessive gene, so it primarily affects boys. Symptoms begin in the legs and include fatigue, difficulty walking, and muscle weakness that gets worse over time and spreads to other muscles. There is no cure, and those affected often require use of a wheelchair by their early teens and don't survive past late teens or early adulthood.More Related Content
Viewers also liked (6)
Autism
AutismMr. Holley's H.I. Classes
油
Autism is a disorder marked by problems with social interaction and communication, as well as restrictive and repetitive behaviors. Some people are born with autism while others develop it later in life. Symptoms typically emerge between ages 2-3 and may include lack of social engagement, delayed language development, and stimming behaviors like hand flapping. While there is no cure, early intervention through specialized education programs can help children with autism improve their communication and learning skills. Providing support is important, as autism often co-occurs with conditions like intellectual disabilities, seizures, or genetic syndromes.Cerebral palsy
Cerebral palsyMr. Holley's H.I. Classes
油
Cerebral palsy is a motor disability caused by abnormal brain development before one month of age that results in a lack of normal movement control. Symptoms may not appear until 9-24 months as the brain areas controlling movement are immature. There is no cure, but physical, occupational, and behavioral therapies can help improve motor skills and independence as well as prevent deformities through medications, braces, and sometimes surgery.Down syndrome
Down syndromeArie Dewi M Arif's
油
Down syndrome is a genetic disorder caused by a full or partial extra copy of chromosome 21. This additional genetic material alters development and causes characteristic physical traits like low muscle tone, small stature, and a single deep crease in the palm. Early intervention through therapies can help children with Down syndrome achieve basic skills and lay a foundation for future progress, as delays are common in areas like physical, cognitive, language, and social development. Education requires careful consideration and supports, though with interventions people with Down syndrome can learn at their own pace and have varied goals and roles.Spina bifida
Spina bifidaMr. Holley's H.I. Classes
油
Spina bifida is a birth defect that results from a mistake early in the development of the spinal cord. It causes symptoms like a bulging spinal cord, hydrocephalus, paralysis in the lower back and legs, and bladder and bowel issues. Spina bifida is a chronic condition meaning it cannot be cured, only treated, through surgery, medication, and physiotherapy. Many people with spina bifida will require assistive devices like braces, crutches, or wheelchairs.Spina bifida
Spina bifidaMr. Holley's H.I. Classes
油
Spina bifida is a birth defect that results from a mistake early in the development of the spinal cord, causing difficulties with feeding, breathing, swallowing, and arm stiffness. There is no known cure for nerve damage from spina bifida, but pediatric neurosurgeons can operate to close openings on the back to prevent further damage and infection. Volunteering at organizations that help people with spina bifida is one way to provide assistance.Down syndrome
Down syndromeMr. Holley's H.I. Classes
油
Down syndrome is a genetic condition that affects mental and physical development. People with Down syndrome may have some recognizable physical features but symptoms vary in severity. Common symptoms include delayed mental development, lack of muscle tone, and a flattened face. Individuals with Down syndrome also have an increased risk of health issues like leukemia, lung infections, Alzheimer's disease, and diabetes. While there is no cure for Down syndrome, educational and physical therapies can help. Genetic counseling may help assess risks for expectant mothers.Similar to Holley (20)
Muscular dystrophy
Muscular dystrophyMr. Holley's H.I. Classes
油
Muscular dystrophy is a group of genetic diseases that progressively weaken muscles without a known cure. Symptoms vary depending on the type but can include muscle weakness, drooping eyelids, difficulty walking, and problems breathing in later stages. Treatment focuses on maintaining range of motion through passive stretching conducted by physical therapists and trained caregivers.Muscular dystrophy presentation
Muscular dystrophy presentationkkbauer
油
Muscular dystrophy is a group of inherited diseases that cause the voluntary muscles to progressively weaken over time. There are nine main types of muscular dystrophy that can affect any age or gender. Symptoms include muscle weakness, spasms, and difficulty with mobility. While there is no cure, treatment aims to relieve symptoms and slow progression through medications, therapy, exercise, and assistive devices. Researchers are working to develop new treatments like gene therapy.Hi power point
Hi power pointMr. Holley's H.I. Classes
油
Muscular dystrophy is a hereditary disease characterized by the gradual wasting of muscles. It sometimes also affects the heart. The symptoms include difficulty using muscle groups, drooping eyelids, frequent falls, and loss of muscle strength and size. Living with muscular dystrophy can make walking difficult and require the use of a wheelchair. It may also necessitate lifelong assistance with daily tasks like feeding. To help those affected, people can volunteer at disability homes by assisting with activities and providing support.Muscular Dystrophy Research Paper
Muscular Dystrophy Research PaperCwintzell1993
油
Muscular dystrophy is a genetic disorder that causes progressive muscle weakness. It is characterized by defects in muscle proteins and affects skeletal, heart and smooth muscles. The main symptoms are muscle weakness and deterioration over time, leading to difficulties with movement. There are many types of muscular dystrophy but they all involve degeneration of muscle fibers. Currently there is no cure, but treatment focuses on managing symptoms and slowing disease progression through exercise, physical therapy and other means. Researchers are working on developing new treatments such as gene therapy.Senior Project Research paper
Senior Project Research paperCwintzell1993
油
Muscular dystrophy is a genetic disorder that causes progressive muscle weakness. It is characterized by defects in muscle proteins and affects skeletal, heart and smooth muscles. The main symptoms are muscle weakness and deterioration over time, leading to difficulties with movement. There are many types of muscular dystrophy but they all involve degeneration of muscle fibers. Currently there is no cure, but treatment focuses on managing symptoms and slowing disease progression through exercise, physical therapy and other means. Researchers are working on developing new treatments such as gene therapy.Gene therapy for muscular dystrophy
Gene therapy for muscular dystrophyMohamed Elasaly, PT, CKTP, MSc Biotech.
油
The document discusses muscular dystrophy, focusing on its historical accounts, symptoms, and gene therapy approaches for treatment. It details the significance of the dystrophin gene and its role in muscular dystrophies, particularly Duchenne and Becker muscular dystrophy. Additionally, various gene therapy strategies, including gene augmentation, genome editing, and exon skipping, are explored as potential treatments for the condition.Muscular (autosaved) orignal
Muscular (autosaved) orignalNandkishor Rautrai
油
Muscular dystrophy is a group of muscle diseases that weaken the musculoskeletal system and hamper movement. There is currently no cure, but physiotherapy, exercise, supplements and medications can help maintain muscle strength. Researchers are investigating recombinant DNA therapies to restore dystrophin production. The document reviews the history, causes, symptoms, types, diagnosis and treatment of muscular dystrophy. Treatment options discussed include medications, physical therapy, surgery and assistive devices.Muscular Dystrophy!!
Muscular Dystrophy!!Jennifer Chora
油
Muscular dystrophy is a genetic disorder that causes muscles to weaken over time due to missing or defective genes preventing the body from producing necessary proteins. There are several types of muscular dystrophy affecting different muscle groups with varying degrees of severity. While there is no cure, treatment aims to preserve muscle and joint function and slow deterioration through therapies, braces, wheelchairs and respiratory support.DUCHENNE MUSCULAR DYSTROPHY
DUCHENNE MUSCULAR DYSTROPHYAniedu Ifeanyichukwu
油
Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle weakness. It is caused by an absence of the protein dystrophin due to mutations in the dystrophin gene on the X chromosome. The disease mainly affects boys and results in the breakdown of skeletal muscles. While there is no cure, treatment aims to manage symptoms and improve quality of life through physical therapy, bracing, medication, and respiratory/nutritional support. Research continues on new therapies such as gene therapy to replace the missing dystrophin protein.Muscular dystrophy
Muscular dystrophyCourtney
油
Muscular dystrophy (MD) is a genetic disease characterized by progressive muscle weakness and degeneration. There are over 30 types of MD that vary in age of onset, progression rate, and pattern of inheritance. The most common forms are Duchenne MD, which affects boys and leads to loss of mobility by age 20, and Becker's MD, which has a slower progression in males. Teachers can support students with MD by making accommodations, encouraging independence and peer interaction, and recommending counseling to help manage the physical and psychological impacts of the disease.mygeneticspresentation-141130173403-conversion-gate02.pptx
mygeneticspresentation-141130173403-conversion-gate02.pptxAnnaKhurshid
油
This document provides an overview of Duchenne muscular dystrophy (DMD). It begins with a brief history of the disease and its discovery. It then discusses the genetic basis and pathophysiology of DMD, which involves a mutation in the dystrophin gene. The clinical features and stages of DMD are outlined, from early ambulatory difficulties in childhood to loss of ambulation and eventual death often by the 30s due to respiratory or cardiac failure. Current treatment focuses on symptom management through physical therapy, bracing, medications, and nutritional support, though stem cell therapy and gene therapy show promise.Muscular Dustropy
Muscular Dustropytamscott5
油
Muscular Dystrophy is a genetic disorder that causes muscle weakness and wasting. It refers to a group of genetic disorders that destroy muscles over time. The most common type is Duchenne Muscular Dystrophy, which affects boys starting between ages 2-6 and causes progressive muscle degeneration and weakness. Eventually, people with DMD may need wheelchairs and ventilators and usually do not survive past their late teens or early adulthood due to heart and respiratory failure. While there is no cure for MD, research is ongoing to help manage symptoms and prolong life.MUSCULAR DYSTROPHY syndrome in child.pptx
MUSCULAR DYSTROPHY syndrome in child.pptxNarayanNeupane3
油
Muscular dystrophy is a group of genetic diseases that causes the muscles to weaken over time. The main symptom is progressive muscle weakness. There are many forms of muscular dystrophy that vary in their severity, affected muscles, age of onset, and progression. While there is no cure, treatment focuses on managing symptoms, slowing disease progression, and maintaining mobility and independence through medications, physical therapy, braces, and other assistive devices.Muscular dystrophy hi
Muscular dystrophy hiMr. Holley's H.I. Classes
油
Muscular dystrophy is a hereditary, progressive, and non-curable disease that causes the degeneration and weakness of skeletal muscles due to defective genes. There are several types of muscular dystrophy including Duchenne and Becker muscular dystrophy, which primarily affects males and can be life-threatening before age 20; limb-girdle dystrophy, which affects both genders and starts in the pelvis and legs; and facioscapulohumeral dystrophy, which relates to muscles in the face, shoulders, and arms. While there is no cure, treatment focuses on physical therapy, exercises, braces, and corrective surgery to relieve symptoms.Presentation2
Presentation2Mr. Holley's H.I. Classes
油
Muscular dystrophy is a genetic disorder that causes progressive muscle weakness and wasting. It is characterized by problems with coordination, mobility, muscle weakness, and joint stiffness. Over time, it can lead to an increased reliance on wheelchairs, crutches, or other mobility assistance as well as potential impacts to breathing and heart function. The specific type and severity of muscular dystrophy depends on the gene defects involved and at what age symptoms first appear.Duchenne Muscular Dystrophy
Duchenne Muscular DystrophyMyzak
油
Duchenne Muscular Dystrophy is a disease that causes rapidly worsening muscle weakness due to a lack of the protein dystrophin. It is inherited through an X-linked recessive gene, so it primarily affects boys. Symptoms begin in the legs and include fatigue, difficulty walking, and muscle weakness that gets worse over time and spreads to other muscles. There is no cure, and those affected often require use of a wheelchair by their early teens and don't survive past late teens or early adulthood.Muscular dystrophy
Muscular dystrophyMr. Holley's H.I. Classes
油
Muscular dystrophy is a hereditary disease that causes the progressive weakening and degeneration of skeletal muscles. Symptoms include muscle weakness, loss of strength, clumsiness and loss of coordination. Long term effects are loss of all muscle control and mobility, with respiratory failure being the cause of death for most patients before age 30. Treatment focuses on physical therapy, braces, surgery and drugs to assist with care, though there is no cure and few patients live beyond 30 due to respiratory failure. Ways to help include providing transportation, lifting assistance, home modifications, and social support.Duchenne's Muscular Dystrophy and Gene Therapy
Duchenne's Muscular Dystrophy and Gene TherapyHercolanium GDeath
油
The document provides an overview of muscular dystrophy, particularly focusing on Duchenne Muscular Dystrophy (DMD), a severe genetic disorder affecting muscle function, primarily caused by the absence of dystrophin protein due to mutations in the dystrophin gene. It highlights the various inheritance patterns, symptoms, and current gene therapy advancements aimed at treating DMD, including antisense techniques and exon skipping methods that could potentially restore dystrophin production in affected individuals. Despite no known cure, the document outlines therapies and ongoing clinical trials exploring the efficacy of gene therapy in managing this condition.Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophymichaela shaffer
油
Duchenne muscular dystrophy is a genetic disorder caused by the absence of the dystrophin protein. It is characterized by progressive muscle degeneration and weakness. Symptoms begin in early childhood and worsen over time, often resulting in the need for a wheelchair in the early teens. While there is no cure, treatment focuses on managing symptoms and complications to improve quality of life. Research is ongoing to develop new treatments such as stem cell therapy and gene therapy.Muscular Dystrophies.pptx
Muscular Dystrophies.pptxRN Yogendra Mehta
油
Muscular dystrophies are a group of incurable muscle disorders characterized by progressive muscle weakening due to gene mutations, primarily affecting the dystrophin gene. Common types include Duchenne, Emery-Dreifuss, and Limb-Girdle muscular dystrophy, each with varying symptoms and inheritance patterns. Diagnosis involves family history, blood tests, and imaging, while treatment options include steroid medications, gene therapy, and supportive therapies.Ad
More from Mr. Holley's H.I. Classes (20)
Autism
AutismMr. Holley's H.I. Classes
油
Autism is a brain disorder that affects communication and social interaction. Some key symptoms include a lack of speech development early on, difficulties reading facial expressions and being socially attentive, and potential learning disabilities or self-harming behaviors of varying severity. The document provides an overview of autism and its characteristics in under three sentences.Down syndrome
Down syndromeMr. Holley's H.I. Classes
油
Down Syndrome is caused by an extra copy of chromosome 21. It is characterized by physical traits like a broad short skull and mental retardation. People with Down Syndrome can have mild, moderate, or severe mental retardation, but with education and training they can still lead independent lives despite their individual strengths and weaknesses. Having severe mental retardation does not mean a person cannot think or feel.Cerebral palsy
Cerebral palsyMr. Holley's H.I. Classes
油
Cerebral palsy is a motor disability caused by abnormal brain development that causes lack of normal movement control and is evident by age 2. Symptoms may not appear until a child tries to walk. Treatment includes physical aids like wheelchairs, walkers and leg braces made of lightweight plastic molded to the body. The document defines cerebral palsy and cites two references on the topic.Cerebral palsy
Cerebral palsyMr. Holley's H.I. Classes
油
Cerebral palsy is a form of paralysis caused by brain damage before or during birth that affects movement and muscle control. It is not a disease but a condition. While there is no cure, treatment and therapy can help improve mobility and daily living. Cerebral palsy symptoms vary but may include problems walking, moving limbs, speaking, and muscle coordination that are noticed before age 2. With proper care, those with cerebral palsy can live independently or in a group home as adults.Holley project
Holley projectMr. Holley's H.I. Classes
油
Down syndrome is a genetic condition characterized by mild to moderate intellectual disabilities and distinctive facial features. It occurs in about 1 in 200 births. Common physical traits include an epicanthic eye fold, excess skin on the neck, and unusual palm creases. There is no specific treatment for Down syndrome, but volunteering can help support individuals who have the condition.Down syndrome
Down syndromeMr. Holley's H.I. Classes
油
Down syndrome is caused by an extra copy of chromosome 21, causing problems with mental retardation, heart and eyesight. People with Down syndrome have distinct facial features and are usually short in stature, as babies with Down syndrome are often born smaller with fewer brain cells. Babies with Down syndrome go through cell therapy.Spina bifida syndrome p3
Spina bifida syndrome p3Mr. Holley's H.I. Classes
油
Spina bifida is a birth defect where the spinal cord fails to develop properly, leaving it exposed or causing deformities. It has no cure and treatment focuses on managing symptoms like bowel and bladder issues. Surgery may be needed to protect exposed tissues, though function cannot be restored to damaged nerves. People with spina bifida require lifelong management to prevent complications and maximize independence through therapies and positive reinforcement.Cerebral palsy
Cerebral palsyMr. Holley's H.I. Classes
油
Cerebral palsy is a condition that affects brain and nervous system functions, impacting movement, learning, and thinking. It is characterized by abnormal gait, loss of muscle movement coordination, speech problems, and potential learning disabilities. While there is no cure for cerebral palsy, victims can live independently or in institutions with treatment including doctors, therapists, braces, and mobility aids. The condition severely disables those affected and makes independent survival difficult without outside assistance.Spina bifida
Spina bifidaMr. Holley's H.I. Classes
油
Spina bifida is a birth defect where the spinal cord fails to develop properly, leaving it exposed. It can cause issues like difficulty swallowing, breathing problems while sleeping, below average intelligence, and more. Research shows repairing spina bifida while still in the womb leads to better outcomes than post-birth surgery. People can help by participating in advocacy efforts, making financial contributions, or volunteering for organizations that support those with spina bifida.Muscular dystrophy
Muscular dystrophyMr. Holley's H.I. Classes
油
Muscular dystrophy is a genetic disorder that causes progressive skeletal muscle weakness. It is characterized by defects in muscle proteins and death of muscle cells and tissue. There is no cure, but treatments include physical therapy, braces, surgery, and drug therapy. It occurs mostly in boys ages 1-4 and the main sign is muscle weakness. Those affected experience a loss of muscle control and mobility over time and most die before age 30 due to respiratory failure.Cerebral palsy
Cerebral palsyMr. Holley's H.I. Classes
油
Cerebral palsy is a permanent condition affecting the brain and nervous system that is present at birth or in early childhood. It causes muscle stiffness, tremors, and problems with movement, balance, and coordination. The most common type is spastic cerebral palsy, which makes muscles stiff and contracted. Patients require lifelong care and physical therapy to help them better move and balance. Caregivers are also needed to assist those with cerebral palsy since they cannot care for themselves without help.Holley project
Holley projectMr. Holley's H.I. Classes
油
Down syndrome is a genetic condition characterized by mild to moderate intellectual disabilities and distinctive facial features. It occurs in about 1 in 200 births. Common physical traits include an epicanthic eye fold, excess skin on the neck, and unusual palm creases. There is no specific treatment for Down syndrome, but volunteering can help support individuals who have the condition.Multiple sclerosis
Multiple sclerosisMr. Holley's H.I. Classes
油
Multiple Sclerosis is a disease where the immune system attacks the protective covering of the nerves, which can damage nerves to the point of losing ability to walk or speak. There is no cure for MS, but treatments include various injections and physical therapy to slow progression, as scientists continue searching for a permanent cure for the disease that affects around 250,000-350,000 people in the United States alone.Multiple sclerosis
Multiple sclerosisMr. Holley's H.I. Classes
油
Multiple Sclerosis is a disease where the immune system attacks the protective covering of the nerves, which can damage nerves to the point of losing ability to walk or speak. There is no cure for MS, but treatments include various injections and physical therapy to slow progression, as scientists continue searching for a permanent cure for the disease that affects around 250,000-350,000 people in the United States alone.Down syndrome
Down syndromeMr. Holley's H.I. Classes
油
Down syndrome is a genetic condition present at birth that affects physical and mental development, causing distinctive facial features and short stature. Approximately 5,000 babies are born with Down syndrome each year in the United States, affecting over 350,000 American families. While there is no cure for Down syndrome, medical treatment focuses on managing associated conditions, and early intervention/therapies help many with Down syndrome live long, productive lives.Autism
AutismMr. Holley's H.I. Classes
油
Autism is a neurobiological disorder characterized by deficits in social interaction and communication as well as abnormal behaviors and activities. Its characteristics include delays in language, play, and social skills as well as repetitive movements. While it causes lifelong impacts like difficulty with social interaction, autism can be treated through structured schedules, special education, speech/occupational/physical therapies, and understanding from others. Though autism causes challenges, many people with autism can be high-functioning and productive members of society.Multiple sclerosis
Multiple sclerosisMr. Holley's H.I. Classes
油
Multiple sclerosis is an autoimmune disease that affects the central nervous system. Symptoms vary and can include visual disturbances, numbness, and impaired mobility. While there is no known cure, treatments can help control symptoms and maintain quality of life. Physical therapy and medications can help manage symptoms and potentially slow progression of the disease. Lifestyle factors like nutrition, rest, and stress management may also help improve quality of life for those living with MS.Down syndrome doesnt suck
Down syndrome doesnt suckMr. Holley's H.I. Classes
油
Down syndrome is a chromosome disorder caused by an extra chromosome 21, resulting in mental retardation and physical characteristics. It is characterized by a flat facial profile, upward slanted eyes, small mouth, and short limbs. With proper medical care, life expectancy has increased to around 55 years. While there are no drugs to treat Down syndrome directly, understanding the affected genes could help address certain symptoms. Parents should educate themselves, engage their child in physical activities, talk to other families of children with Down syndrome, and ensure their child attends regular medical appointments and receives all vaccinations. People can help kids with Down syndrome by participating in activities like Special Olympics.Down syndrome
Down syndromeMr. Holley's H.I. Classes
油
Down syndrome is a genetic disorder caused by the presence of an extra chromosome 21. It is associated with intellectual disabilities, distinctive facial features, and health issues. Individuals with Down syndrome often have heart defects, intestinal abnormalities, vision or hearing problems, infections, thyroid issues, or an increased risk of leukemia. Long-term effects include these medical conditions as well as memory loss. Infants require more assistance than older individuals with Down syndrome due to increased risk of infections. People can help by volunteering at facilities that care for children with Down syndrome.Multiple sclerosis
Multiple sclerosisMr. Holley's H.I. Classes
油
Multiple sclerosis (MS) is a progressive disease of the central nervous system characterized by destruction of the myelin sheath surrounding nerve fibers in the brain, spinal cord, and optic nerves. This impairs nerve signal transmission, especially for vision, sensation, and movement. MS is diagnosed through MRI scans of the spinal cord and brain detecting lesions. While there is no cure for MS, effective treatments exist to help manage its lifelong effects on the nervous system.Ad
Holley
- 1. Muscular Dystrophy Nick Cervantes Mr. Holley H.I. Spring 2011 http://moblog.whmsoft.net/shared_images/en/image003_2999b163b7841f6de94f4ac872d23d48.jpg
- 2. Definition In muscular dystrophy, muscles become progressively weaker. As individual muscle fibers become so weak that they die, they are replaced by connective tissue, which is fibrous and fatty rather than muscular tissue (Karen E. Kalumuck, Ph.D.L. Fleming Fallon, Jr.)
- 3. Symptoms Weakness in the hips and upper thighs Intelligence Reduction http://www.medindia.net/health-images/Duchenne-Muscular-Dystrophy-is-Ultimately-a-Stem-Cell-Disease@@colorful-cells.jpg
- 4. Life Long Effects Disability to walk by early teens Abnormal bone development Possible paralysis Death by mid 20s
- 5. Treatment There is no known cure currently Respiratory aid Physical Therapy
- 6. How can I help someone with MD I could volunteer to help someone with muscular dystrophy. http://images.clipartof.com/thumbnails/15298-Blue-Person-Pushing-Another-Person-In-A-Wheelchair-In-A-Hospital-Clipart-Illustration-Image.jpg
- 7. Works Cited http://www.medindia.net/news/Duchenne-Muscular-Dystrophy-is-Ultimately-a-Stem-Cell-Disease-77907-1.htm Kalumuck, Karen E. "Muscular dystrophy." Magills Medical Guide, Sixth Edition . Ed. Tracy Irons-Georges, 6th ed. 6 vols. Pasadena, Calif.: Salem Press, 2010. Salem Health Web. 07 Apr. 2011 http://www.britannica.com/EBchecked/topic/398719/muscular-dystrophy