Orthopedic disorders were summarized including:
1. Club foot, juvenile rheumatoid arthritis, hip displacement, fractures, osteomyelitis, kyphosis, scoliosis, lordosis, bow leg, knock knee, polydactyly, and syndactyly were defined and their causes, clinical manifestations, and management were described.
2. Various orthopedic conditions like club foot, hip displacement, fractures are managed through medical and surgical interventions along with nursing care including immobilization, exercise, skin care, and patient/family education.
3. Genetic and developmental factors can cause certain orthopedic disorders while trauma, infections, and nutritional deficiencies also contribute to conditions affecting the
This document provides information about clubfoot including its definition, types, incidence, etiology, clinical manifestations, diagnostics, management, and nursing management. Clubfoot is a congenital deformity where the foot is twisted out of its normal position. It most commonly presents as talipes equinovarus. The incidence is approximately 1 in 1000 live births and it is more common in males. Etiology is multifactorial and can be related to genetic and environmental factors. Types include talipes varus, valgus, equinus, and calcaneus. Management involves medical treatment including manipulation and casting or surgical procedures like soft tissue releases or bony corrections. Nursing care focuses on preventing skin breakdown and managing parental anxiety.
Sprengel's deformity and congenital muscular torticollis are congenital musculoskeletal conditions. Sprengel's deformity involves an elevated scapula due to interrupted migration during development. It causes limited shoulder movement and deformity. Congenital muscular torticollis is caused by sternocleidomastoid muscle shortening, resulting in head tilt and facial asymmetry. Both are typically noticed at birth and can be treated conservatively or with surgery depending on severity. Physiotherapy focuses on improving range of motion and muscle strength.
1. The document discusses various skeletal and limb anomalies that can be detected on prenatal ultrasound, including skeletal dysplasias, dysostoses, and disruptions.
2. Some of the most common skeletal dysplasias discussed are achondroplasia, achondrogenesis, osteogenesis imperfecta, and thanatophoric dysplasia.
3. Ultrasound findings of various anomalies are provided, along with descriptions of specific conditions like achondroplasia, achondrogenesis, osteogenesis imperfecta, and thanatophoric dysplasia. Prognosis and inheritance patterns are also summarized for some conditions.
The document provides information about Club foot, Congenital Hip Dysplasia, and Fractures that was taught to nursing students. Key points include definitions, types, causes, symptoms, diagnostic tests and management for each condition. Students learned to define, explain, list, enumerate, and describe various aspects of Club foot, Congenital Hip Dysplasia, and Fractures.
Clubfoot is a birth defect where one or both feet are twisted into an abnormal position. It is caused by genetic and environmental factors and affects males more than females. Treatment involves stretching the feet into correct position with casting or taping and bracing to maintain correction. Parents are taught exercises and bracing is worn long-term to prevent recurrence. Nursing focuses on monitoring for skin issues from casting, teaching parents exercises and brace use, and supporting the child's development.
This document discusses congenital hip dislocation, including its definition, classification, degrees, etiology, risk factors, clinical manifestations, diagnostic evaluation, and management. Congenital hip dislocation refers to a hip with no contact between the femoral head and acetabulum. It can be classified as typical or teratologic. Degrees include acetabular dysplasia, subluxation, and dislocation. Risk factors include family history, gender, breech position, and oligohydramnios. Diagnosis involves history, physical exam, ultrasound, and x-rays. Management depends on age, and may include closed/open reduction and casting or bracing.
This document provides an overview of examining the neck and various neck deformities. It begins with a brief anatomy section covering the bones and structures of the neck. It then outlines the steps to examine the neck - looking at the neck from all angles, feeling the bony contours and muscles, and moving the neck through its range of motion. Various neck deformities are classified and described, including congenital torticollis, Klippel-Feil syndrome, congenital high scapula, and ankylosing spondylitis. Treatment options are mentioned for each condition. Special tests to evaluate neurological involvement are also outlined.
Clubfoot is a congenital condition where one or both feet are twisted into an abnormal position at birth. It occurs in about 1 in 1,000 live births and is more common in males. The cause is abnormal foot development in the uterus. Treatment involves gradually correcting the deformity with casts and splints, followed by exercises to maintain the correction and prevent recurrence. Nursing care focuses on monitoring for skin breakdown and impaired circulation during casting, teaching parents how to care for the child, and addressing psychosocial impacts of the condition.
Pierre Robin syndrome is a condition characterized by three components: cleft palate, mandibular micrognathia or retrognathia, and glossoptosis. It is caused by the mechanical theory where cleft palate prevents palatal shelf fusion and mandibular hypoplasia constrains growth, leading to tongue displacement. Achondroplasia is caused by mutations affecting endochondral ossification, leading to disproportionate short stature and limb shortening, large head size, and restricted joint motion. Both conditions are diagnosed based on clinical features and imaging findings, and require multidisciplinary care.
The document discusses various types of congenital and acquired deformities of the human body. It describes two main types of deformities - congenital, which are present at birth, and acquired, which develop after birth. For congenital deformities, it provides examples affecting the shoulder, elbow, wrist, and hand. These include conditions like spangel's shoulder, congenital dislocation of the elbow, carpal fusions, and radial/ulnar club hand. It also discusses classifications of deformities based on their severity and treatments for some common congenital conditions.
This document discusses various angular deformities of the knee, including genu varum (bowlegged), genu valgus (knock-kneed), genu recurvatum, and genu procurvatum. It provides details on the causes, presentations, treatments, and assessments of genu varum and genu valgus. For genu varum, treatment may involve observation, bracing, or osteotomy, while genu valgus can be treated with observation, bracing, hemiepiphysiodesis, or osteotomy in more severe cases. Assessments involve measurements like intermalleolar distance and Q angle to evaluate deformities.
This document discusses developmental dysplasia of the hip (DDH), which refers to abnormal development of the hip joint that can occur before or after birth. DDH ranges in severity from mild acetabular dysplasia to complete dislocation of the femoral head. Risk factors include family history, female sex, breech positioning, and tight uterine environments. Symptoms vary by age but may include limping, leg length discrepancy, or limited hip abduction. Diagnosis involves physical exam maneuvers and imaging tests. Treatment depends on age and severity, and may include closed or open reduction along with casting or bracing to maintain proper hip positioning. Complications can include avascular necrosis or joint damage if not properly treated.
Paediatric MSK problems
Signs and symptoms
MSK signs and symptoms:
Limp.
Joint pain and swelling.
Remember that hip pain may be referred to the knee.
Morning stiffness.
Gelling: stiffness following period of inactivity.
Weakness and instability.
Pseudoparalysis: limb fixed in pain.
Associated systemic symptoms:
Fever
Feeding or growth.
Rash.
Poor sleep.
History of trauma:
Incongruous signs might suggest non-accidental injury.
Functional limitations.
Differential diagnosis
General:
First exclude trauma which may be missed/unwitnessed (especially in young e.g. toddler's fracture) and infection septic arthritis, osteomyelitis, or discitis.
Consider general causes of MSK pain such as growing pains (often nocturnal), hypermobility, and complex regional pain syndrome.
Acute: irritable hip, neuroblastoma, leukaemia.
Chronic: developmental dysplasia of the hip, talipes, cerebral palsy, juvenile idiopathic arthritis (JIA).
ADACTYLY IN FETUS
PORENCEPHALIC CYST IN FETUS
SEPTO-OPTIC DYSPLASIA IN FETUS
MUSCLE HERNIA IN ADULT
FETAL REDUCTION
AGENESIS OF CORPUS CALLOSUM
FLAT FETAL FACIAL PROFILE
Congenital talipes equinovarus, or clubfoot, is a common birth defect where the foot is twisted out of shape. It occurs in about 1 in 1000 births and is more common in males. Genetic factors are believed to play a role. Treatment usually begins within the first weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Properly fitted braces are then worn long term to maintain the corrected position and allow normal walking. With early treatment, most children with clubfoot can walk normally.
This document discusses congenital talipes equinovarus, or clubfoot, which is a common birth defect where the foot is twisted out of shape. It occurs in about 1 in 1000 births. Clubfoot is usually an isolated problem in otherwise healthy newborns and is twice as common in males. Treatment typically begins within the first weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Proper use of braces after treatment is needed to prevent the foot from returning to its original position. The cause is usually unknown but genetics and environmental factors may play a role. Nursing care focuses on supporting parents, educating on treatment and self-care, and protecting the skin during casting.
1. A skeletal dysplasia is a congenital abnormality of bone growth or development that results in structural abnormalities of the bones.
2. Making a diagnosis involves taking a thorough history and physical examination, including measurements of height, limb lengths, and facial features. Radiographs can identify which bones are affected.
3. Achondroplasia is the most common skeletal dysplasia, caused by a mutation in the FGFR3 gene, and is characterized by disproportionate short stature, frontal bossing, trident hands, genu varum, and foramen magnum stenosis.
SKELETAL DISORDERS AMONG CHILDREN BY NASIR AHMADNASIR AHMAD
油
This document provides information on congenital talipes equinovarus, or clubfoot, which is a common birth defect where the foot is twisted out of shape. It affects about 1 in 1000 births. Clubfoot is caused by shortened tendons in the foot and can be either idiopathic (no known cause) or associated with genetic factors or other conditions. Treatment typically begins within the first few weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Proper bracing after treatment is needed to prevent recurrence. The document outlines nursing assessments and care goals for managing clubfoot.
This document provides an overview of orthopedic surgery and musculoskeletal symptoms and examination. It discusses the history and origins of orthopedics, describes common orthopedic symptoms like pain, stiffness, swelling, and deformity. It then outlines the process of examining a musculoskeletal patient, including inspection, palpation, and assessing range of motion and muscle strength. Various joint types are also classified, including fibrous, cartilaginous, and synovial joints. Synovial joints are described in further detail.
The document discusses orthopedic surgery and provides details on:
- The history and origins of orthopedics as a field dealing with deformities, bone/joint diseases, and musculoskeletal injuries
- Common symptoms in orthopedics such as pain, stiffness, swelling, and deformity
- The typical examination process for orthopedic issues including inspection, palpation, and assessing range of motion and tests
- Key terminology used in orthopedics to describe anatomical planes, directions, alignments, and types of deformities
The document discusses the embryology of the upper limb and hand development. It notes that between 5-8 weeks of gestation is the critical period for limb development. The zones of polarizing activity and apical ectodermal ridge play important roles in directing growth. Thumb hypoplasia is often associated with radial deficiencies and other syndromes. The document covers classifications of thumb hypoplasia and radial deficiencies and discusses evaluation and treatment considerations.
The document discusses congenital hand anomalies, beginning with definitions and embryology. It describes how hand development begins in the 4th week after fertilization and is guided by three signaling centers. Classification systems for congenital hand anomalies are discussed, including Swanson's classification which is based on embryologic origin and morphology. The types of anomalies covered include failure of formation (transverse arrest, longitudinal arrest, radial/ulnar club hand, cleft hand), failure of differentiation (syndactyly), and duplication (polydactyly). Specific examples and classifications of different anomalies are provided.
Developmental dysplasia of the hip (DDH) is a spectrum of disorders involving abnormal development of the hip joint that may present as dysplasia, subluxation, or dislocation. It results from excessive laxity of the hip capsule allowing the femoral head to slip out of the acetabulum. DDH is diagnosed through clinical examination including Ortolani and Barlow's tests in infants, and imaging such as ultrasound and x-rays. Treatment depends on the degree of hip involvement and age of presentation, ranging from bracing to closed or open reduction. Screening of newborns is important for early detection and management to prevent long-term complications.
Blount's disease, also known as tibia vara, is a progressive orthopedic condition that causes bowing of the legs in children. It results from a growth disturbance in the proximal medial tibial growth plate. The deformity includes varus alignment of the knees, internal tibial torsion, and leg length discrepancy. Radiographs show a characteristic wedging and irregularity of the proximal medial tibial epiphysis. Treatment depends on age and severity, ranging from bracing to corrective osteotomies. Congenital metatarsus adductus is another common pediatric foot deformity involving inward twisting of the forefoot. It is often mild and resolves with stretching, but more severe cases may require
This document provides an overview of arthrogryposis multiplex congenita (AMC), including:
1) A definition of AMC as a nonprogressive condition characterized by multiple joint contractures present at birth involving at least two body regions.
2) A discussion of classification systems and the etiology, which is usually absence of fetal movement leading to contractures.
3) Details on clinical features including common joint involvement in the upper and lower limbs, classification of distal arthrogryposis types, and other arthrogryposis conditions.
This document provides an overview of examining the neck and various neck deformities. It begins with a brief anatomy section covering the bones and structures of the neck. It then outlines the steps to examine the neck - looking at the neck from all angles, feeling the bony contours and muscles, and moving the neck through its range of motion. Various neck deformities are classified and described, including congenital torticollis, Klippel-Feil syndrome, congenital high scapula, and ankylosing spondylitis. Treatment options are mentioned for each condition. Special tests to evaluate neurological involvement are also outlined.
Clubfoot is a congenital condition where one or both feet are twisted into an abnormal position at birth. It occurs in about 1 in 1,000 live births and is more common in males. The cause is abnormal foot development in the uterus. Treatment involves gradually correcting the deformity with casts and splints, followed by exercises to maintain the correction and prevent recurrence. Nursing care focuses on monitoring for skin breakdown and impaired circulation during casting, teaching parents how to care for the child, and addressing psychosocial impacts of the condition.
Pierre Robin syndrome is a condition characterized by three components: cleft palate, mandibular micrognathia or retrognathia, and glossoptosis. It is caused by the mechanical theory where cleft palate prevents palatal shelf fusion and mandibular hypoplasia constrains growth, leading to tongue displacement. Achondroplasia is caused by mutations affecting endochondral ossification, leading to disproportionate short stature and limb shortening, large head size, and restricted joint motion. Both conditions are diagnosed based on clinical features and imaging findings, and require multidisciplinary care.
The document discusses various types of congenital and acquired deformities of the human body. It describes two main types of deformities - congenital, which are present at birth, and acquired, which develop after birth. For congenital deformities, it provides examples affecting the shoulder, elbow, wrist, and hand. These include conditions like spangel's shoulder, congenital dislocation of the elbow, carpal fusions, and radial/ulnar club hand. It also discusses classifications of deformities based on their severity and treatments for some common congenital conditions.
This document discusses various angular deformities of the knee, including genu varum (bowlegged), genu valgus (knock-kneed), genu recurvatum, and genu procurvatum. It provides details on the causes, presentations, treatments, and assessments of genu varum and genu valgus. For genu varum, treatment may involve observation, bracing, or osteotomy, while genu valgus can be treated with observation, bracing, hemiepiphysiodesis, or osteotomy in more severe cases. Assessments involve measurements like intermalleolar distance and Q angle to evaluate deformities.
This document discusses developmental dysplasia of the hip (DDH), which refers to abnormal development of the hip joint that can occur before or after birth. DDH ranges in severity from mild acetabular dysplasia to complete dislocation of the femoral head. Risk factors include family history, female sex, breech positioning, and tight uterine environments. Symptoms vary by age but may include limping, leg length discrepancy, or limited hip abduction. Diagnosis involves physical exam maneuvers and imaging tests. Treatment depends on age and severity, and may include closed or open reduction along with casting or bracing to maintain proper hip positioning. Complications can include avascular necrosis or joint damage if not properly treated.
Paediatric MSK problems
Signs and symptoms
MSK signs and symptoms:
Limp.
Joint pain and swelling.
Remember that hip pain may be referred to the knee.
Morning stiffness.
Gelling: stiffness following period of inactivity.
Weakness and instability.
Pseudoparalysis: limb fixed in pain.
Associated systemic symptoms:
Fever
Feeding or growth.
Rash.
Poor sleep.
History of trauma:
Incongruous signs might suggest non-accidental injury.
Functional limitations.
Differential diagnosis
General:
First exclude trauma which may be missed/unwitnessed (especially in young e.g. toddler's fracture) and infection septic arthritis, osteomyelitis, or discitis.
Consider general causes of MSK pain such as growing pains (often nocturnal), hypermobility, and complex regional pain syndrome.
Acute: irritable hip, neuroblastoma, leukaemia.
Chronic: developmental dysplasia of the hip, talipes, cerebral palsy, juvenile idiopathic arthritis (JIA).
ADACTYLY IN FETUS
PORENCEPHALIC CYST IN FETUS
SEPTO-OPTIC DYSPLASIA IN FETUS
MUSCLE HERNIA IN ADULT
FETAL REDUCTION
AGENESIS OF CORPUS CALLOSUM
FLAT FETAL FACIAL PROFILE
Congenital talipes equinovarus, or clubfoot, is a common birth defect where the foot is twisted out of shape. It occurs in about 1 in 1000 births and is more common in males. Genetic factors are believed to play a role. Treatment usually begins within the first weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Properly fitted braces are then worn long term to maintain the corrected position and allow normal walking. With early treatment, most children with clubfoot can walk normally.
This document discusses congenital talipes equinovarus, or clubfoot, which is a common birth defect where the foot is twisted out of shape. It occurs in about 1 in 1000 births. Clubfoot is usually an isolated problem in otherwise healthy newborns and is twice as common in males. Treatment typically begins within the first weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Proper use of braces after treatment is needed to prevent the foot from returning to its original position. The cause is usually unknown but genetics and environmental factors may play a role. Nursing care focuses on supporting parents, educating on treatment and self-care, and protecting the skin during casting.
1. A skeletal dysplasia is a congenital abnormality of bone growth or development that results in structural abnormalities of the bones.
2. Making a diagnosis involves taking a thorough history and physical examination, including measurements of height, limb lengths, and facial features. Radiographs can identify which bones are affected.
3. Achondroplasia is the most common skeletal dysplasia, caused by a mutation in the FGFR3 gene, and is characterized by disproportionate short stature, frontal bossing, trident hands, genu varum, and foramen magnum stenosis.
SKELETAL DISORDERS AMONG CHILDREN BY NASIR AHMADNASIR AHMAD
油
This document provides information on congenital talipes equinovarus, or clubfoot, which is a common birth defect where the foot is twisted out of shape. It affects about 1 in 1000 births. Clubfoot is caused by shortened tendons in the foot and can be either idiopathic (no known cause) or associated with genetic factors or other conditions. Treatment typically begins within the first few weeks of life and involves casting and stretching to realign the foot, sometimes with minor surgery. Proper bracing after treatment is needed to prevent recurrence. The document outlines nursing assessments and care goals for managing clubfoot.
This document provides an overview of orthopedic surgery and musculoskeletal symptoms and examination. It discusses the history and origins of orthopedics, describes common orthopedic symptoms like pain, stiffness, swelling, and deformity. It then outlines the process of examining a musculoskeletal patient, including inspection, palpation, and assessing range of motion and muscle strength. Various joint types are also classified, including fibrous, cartilaginous, and synovial joints. Synovial joints are described in further detail.
The document discusses orthopedic surgery and provides details on:
- The history and origins of orthopedics as a field dealing with deformities, bone/joint diseases, and musculoskeletal injuries
- Common symptoms in orthopedics such as pain, stiffness, swelling, and deformity
- The typical examination process for orthopedic issues including inspection, palpation, and assessing range of motion and tests
- Key terminology used in orthopedics to describe anatomical planes, directions, alignments, and types of deformities
The document discusses the embryology of the upper limb and hand development. It notes that between 5-8 weeks of gestation is the critical period for limb development. The zones of polarizing activity and apical ectodermal ridge play important roles in directing growth. Thumb hypoplasia is often associated with radial deficiencies and other syndromes. The document covers classifications of thumb hypoplasia and radial deficiencies and discusses evaluation and treatment considerations.
The document discusses congenital hand anomalies, beginning with definitions and embryology. It describes how hand development begins in the 4th week after fertilization and is guided by three signaling centers. Classification systems for congenital hand anomalies are discussed, including Swanson's classification which is based on embryologic origin and morphology. The types of anomalies covered include failure of formation (transverse arrest, longitudinal arrest, radial/ulnar club hand, cleft hand), failure of differentiation (syndactyly), and duplication (polydactyly). Specific examples and classifications of different anomalies are provided.
Developmental dysplasia of the hip (DDH) is a spectrum of disorders involving abnormal development of the hip joint that may present as dysplasia, subluxation, or dislocation. It results from excessive laxity of the hip capsule allowing the femoral head to slip out of the acetabulum. DDH is diagnosed through clinical examination including Ortolani and Barlow's tests in infants, and imaging such as ultrasound and x-rays. Treatment depends on the degree of hip involvement and age of presentation, ranging from bracing to closed or open reduction. Screening of newborns is important for early detection and management to prevent long-term complications.
Blount's disease, also known as tibia vara, is a progressive orthopedic condition that causes bowing of the legs in children. It results from a growth disturbance in the proximal medial tibial growth plate. The deformity includes varus alignment of the knees, internal tibial torsion, and leg length discrepancy. Radiographs show a characteristic wedging and irregularity of the proximal medial tibial epiphysis. Treatment depends on age and severity, ranging from bracing to corrective osteotomies. Congenital metatarsus adductus is another common pediatric foot deformity involving inward twisting of the forefoot. It is often mild and resolves with stretching, but more severe cases may require
This document provides an overview of arthrogryposis multiplex congenita (AMC), including:
1) A definition of AMC as a nonprogressive condition characterized by multiple joint contractures present at birth involving at least two body regions.
2) A discussion of classification systems and the etiology, which is usually absence of fetal movement leading to contractures.
3) Details on clinical features including common joint involvement in the upper and lower limbs, classification of distal arthrogryposis types, and other arthrogryposis conditions.
Blind spots in AI and Formulation Science, IFPAC 2025.pdfAjaz Hussain
油
The intersection of AI and pharmaceutical formulation science highlights significant blind spotssystemic gaps in pharmaceutical development, regulatory oversight, quality assurance, and the ethical use of AIthat could jeopardize patient safety and undermine public trust. To move forward effectively, we must address these normalized blind spots, which may arise from outdated assumptions, errors, gaps in previous knowledge, and biases in language or regulatory inertia. This is essential to ensure that AI and formulation science are developed as tools for patient-centered and ethical healthcare.
Information Technology for class X CBSE skill SubjectVEENAKSHI PATHAK
油
These questions are based on cbse booklet for 10th class information technology subject code 402. these questions are sufficient for exam for first lesion. This subject give benefit to students and good marks. if any student weak in one main subject it can replace with these marks.
How to Setup WhatsApp in Odoo 17 - Odoo 際際滷sCeline George
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Integrate WhatsApp into Odoo using the WhatsApp Business API or third-party modules to enhance communication. This integration enables automated messaging and customer interaction management within Odoo 17.
Digital Tools with AI for e-Content Development.pptxDr. Sarita Anand
油
This ppt is useful for not only for B.Ed., M.Ed., M.A. (Education) or any other PG level students or Ph.D. scholars but also for the school, college and university teachers who are interested to prepare an e-content with AI for their students and others.
Prelims of Rass MELAI : a Music, Entertainment, Literature, Arts and Internet Culture Quiz organized by Conquiztadors, the Quiz society of Sri Venkateswara College under their annual quizzing fest El Dorado 2025.
Research & Research Methods: Basic Concepts and Types.pptxDr. Sarita Anand
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This ppt has been made for the students pursuing PG in social science and humanities like M.Ed., M.A. (Education), Ph.D. Scholars. It will be also beneficial for the teachers and other faculty members interested in research and teaching research concepts.
Useful environment methods in Odoo 18 - Odoo 際際滷sCeline George
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Blind Spots in AI and Formulation Science Knowledge Pyramid (Updated Perspect...Ajaz Hussain
油
This presentation delves into the systemic blind spots within pharmaceutical science and regulatory systems, emphasizing the significance of "inactive ingredients" and their influence on therapeutic equivalence. These blind spots, indicative of normalized systemic failures, go beyond mere chance occurrences and are ingrained deeply enough to compromise decision-making processes and erode trust.
Historical instances like the 1938 FD&C Act and the Generic Drug Scandals underscore how crisis-triggered reforms often fail to address the fundamental issues, perpetuating inefficiencies and hazards.
The narrative advocates a shift from reactive crisis management to proactive, adaptable systems prioritizing continuous enhancement. Key hurdles involve challenging outdated assumptions regarding bioavailability, inadequately funded research ventures, and the impact of vague language in regulatory frameworks.
The rise of large language models (LLMs) presents promising solutions, albeit with accompanying risks necessitating thorough validation and seamless integration.
Tackling these blind spots demands a holistic approach, embracing adaptive learning and a steadfast commitment to self-improvement. By nurturing curiosity, refining regulatory terminology, and judiciously harnessing new technologies, the pharmaceutical sector can progress towards better public health service delivery and ensure the safety, efficacy, and real-world impact of drug products.
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Odoo, a versatile and integrated business management software, excels with its robust Point of Sale (POS) module. This guide delves into the intricacies of configuring restaurants in Odoo 17 POS, unlocking numerous possibilities for streamlined operations and enhanced customer experiences.
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In this slide, well discuss on how to attach file using upload button Odoo 18. Odoo features a dedicated model, 'ir.attachments,' designed for storing attachments submitted by end users. We can see the process of utilizing the 'ir.attachments' model to enable file uploads through web forms in this slide.
2. CLEFT LIP AND CLEFT
PALATE
Presented by: Ms Kajal
M.Sc.N1st
yr
3. INTRODUCTION
It is a congenital malformation resulting from the failure
of fusion of maxillary process during intrauterine
development.
This defect may occur alone or together.
4. Definition
CLEFT LIP (CHEILOSCHISIS): It is result from failure of fusion of
maxillary process with nose elevation on frontal prominence.
TYPES :
1. Partial / incomplete
2. Complete
3. Bilateral
4. Unilateral
5. CLEFT PALATE ( PALATOSCHISIS)
Its result from failure to fusion
of the hard palate with each
other and with the soft palate,
cleft lip usually occurs with
cleft palate.
TYPES:
1. Complete
2. Incomplete.
7. ETIOLOGY / Causes
Medication taken by mother. ( Ex- antimalarial,
anticonvulsion).
Exposure of virus or chemicals.
Maternal anemia
Alcohol abuse
Maternal smoking
13. LOGANS BOW:
As part of a cleft lip
management to
maintain
postoperative
apposition and to
avoid excessive strain
after cheiloplasty for
a cleft lip.
14. MEDICAL MANAGEMENT.
Antibiotics and analgesic.
NURSING MANAGEMENT:
Maintaining adequate nutrition.
Increasing family coping.
Reducing the parents anxiety and guilt regarding
the newborns physical defects,
preparing parents for the future repair of the
cleft lip and palate
15. DEVELOPMENTAL DYSPLASIA OF HIP
DEFINITION: Its id refers to a variety of condition in which
the head of femur and acetabulum cavity are improperly
aligned and the femur head lies outside the hip socket or
acetabulum cavity.
DEGREE OF DDH
1. ACETABULAR DYSPLASIA OR PRELUXATION: mild
dislocation of hip joint to the acetabulum cavity.
2. SUBLUXATION : incomplete dislocation of hip joint.
3. COMPLETE DISLOCATION AND LUXATION : Complete
dislocation of hip joint.
16. ETIOLOGY
common in females than male.
Genetic factors.
Intrauterine position.
Maternal factors.
CLINICAL EVALUATION
Shorting of legs.
Asymmetry of legs.
Gait abnormalities.
17. DIAGNOSIS
BARLOW TEST
ORTOLANI
USG AND X- RAYS.
MANAGEMENT:
Pavlik harness
Brace- Von Rosen splint.
SUREGERY: Closed reduction under
general anesthesia.
NURSING MANAGEMENT
Maintain correct position of hip.
Maintain physical mobility
Educate and support parents.
18. CLUBFOOT (VARUS EQUINUS)
DEFINITION: A common deformity in which the foot is twisted out of its normal shape
or position.
Involving the ankle is known as TALIPES derived TALUS means ankle and PES means
FOOT.
TYPES:
1.TALIPES VARUS : There is an inversion or bending inward of foot.
2.TALIPES VALGUS: There is an eversion or bending outward of foot.
3.TALIPES EQUINUS: There is planter flexion and toes is lower than heel.
4.TALIPES CALCANEOUS: There is dorsiflexion and toes is higher than heel.
20. ETIOLOGY
Monozygotic twins
Genetic factors
Unknown
Teratogen
CLINICAL FEATURES
Adduction of forefoot.
Development of lower legs is also affected.
Difficulty in walking and running
21. MANAGEMENT
NON-OPERATIVE MANAGEMENT :
Casting and splinting.
OPERATIVE MANAGEMENT:
SALVAGE PROCEDURE: Tarsectomy ( removing one or more of the bone of
the tarsus).
NURSING MANAGEMENT:
Maintain skin integrity
Family support
Promote healthy healing.
22. FRACTURE
DEFINITION: A break in the continuity of bone caused by trauma ,
twisting as a result of muscles spasm or indirect impairment of function
and bone decalcification.
CAUSES:
Increase mobility.
Insatiable curiosity.
Immature level of motor coordination.
Lack of calcium
Fall from height
Road traffic accident
23. CLASSIFICATION OF FRACTURE
Based on communication :
1. SIMPLE/ CLOSED FRACTURE.
2. COMPOUND/ OPEN FRACTURE.
3. COMPLETE FRACTURE.
4. INCOMPLETE FRACTURE.
5. SIMPLE/ CLOSED FRACTURE: Skin over the fracture are remain intact.
6. COMPOUND /OPEN FRACTURE: Bone is exposed destroy the continuity of the
bone.
7. COMPLETE FRACTURE: bone is broken across entirely, destroying continuity
of bone.
8. INCOMPLETE FRACTURE: Does not broken completely and destroy continuity
of bone.
24. CLASSIFICATION ON THE BASIC OF PATTERN
TRANSVERSE FRACTURE: Bone is fracture straight across.
OBLIQUE FEACTURE: Break extends in an oblique
direction.
SPIRAL FRACTURE: Spiral fracture in which bone has been
twisted apart.
LINEAR FRACTURE: The bone is fracture longitudinally
25. CLINICAL FEATURE
5P
PAIN
PALLOR
PULSE
PARESTHESIA
PARALYSIS
OTHER; SWELLING, MUSCLES SPASM,BRUISING.
DIAGNOSIS:
Complete history
X ray or CT scan
Lab diagnosis.
26. COMMON SITES OF FRACTURE IN CHILDREN
Clavicle
Humerus
Radius and ulna
Femur
PROCESS OF BONE HEALING
STAGE I: HEMATOMA FORMATION
STAGE II: FIBRO CARTILAGE FORMATION
STAGE III: CALLUS FORMATION
STAGE IV: OSSIFICATION
STAGE V : CONSOLIDATION AND REMODELILING
27. MANAGEMENT
FRACTURE REDUCTION
CAST
TRACTION
NURSING MANAGEMENT:
Promote comfort
Maintain skin integrity
To reduce pain
Provide adequate fluid and nutrient.
28. DISORDERS OF SPINAL CORD
Spine has three types of curve:
1.KYPHOSIS
2.LORDOSIS
3.SCOLIOSIS
1.KYPHOSIS: It is a curving of the spine that cause a bowing or rounding of the
back, which leads to a hunchback or slouching posture.
ETIOLOGY:
Certain endocrine disorder.
Connective tissue disorder
Infection ( POTS SPINE).
Poliomyelitis.
Spina bifida
29. CLINICAL FEATURES:
Difficulty in breathing.
Fatigue.
Mild back pain
Round back appearance
Tenderness and stiffness in the spine.
DIAGNOSIS:
X- ray.
PFT (pulmonary function test).
MRI
31. LORDOSIS
Inward curvature of a portion of the lumbar and cervical vertebral
column.
ETIOLOGY:
Congenital
Neuromuscular problems.
Surgery of spine.
CLINICAL FEATURES:
Prominence of the buttocks.
Back pain
Pain down the legs.
32. MANAGEMENT:
Physiotheraphy
Bracing stabilizing
Orthoplast jacket
NURSING MANAGEMENT:
Assist for theraphy
Counselling
Psychological support
33. SCOLIOSIS
Lateral curve of the spine, generally a sideway curve
greater than 10 degree is considered scoliosis.
ETIOLOGY:
Congenital.
Neuromuscular disorders
Idiopathic causes
CLINICAL FEATURES:
Backpain
Fatique