ݺߣshows by User: EbiweniLokoja / http://www.slideshare.net/images/logo.gif ݺߣshows by User: EbiweniLokoja / Wed, 29 Mar 2017 20:40:40 GMT ݺߣShare feed for ݺߣshows by User: EbiweniLokoja IMMUNODEFICIENCY IN HAEMATOLOGY /slideshow/immunodeficiency-in-haematology/73907371 jamesebi-170329204041
Immunodeficiency refers to failure of immune system to encounter infections by different microbial pathogens such as fungi, bacteria, viruses and protozoan. There are two types of immunodeficiency, Primary immunodeficiency disorder (genetic) and Secondary immunodeficiency disorder (acquired). Primary immunodeficiency disorders (PID) are genetic or inherited disorders which make an individual more susceptible to any pathogenic infections. One in two thousands (2,000) children younger than 18 years are thought to have primary immunodeficiency disorder. Antibody, combined B-cell and T-cell, phagocyte and complement disorders are the most common types. Secondary immunodeficiency disorders (SID) arise due to factors such as malnutrition, fatigue, use of immunosuppressants, chemotherapy, skin damage, pregnancy, aging, and recurrent infections. Laboratory screening test for individuals with immunodeficiency disorders include a complete blood count with differential and measurement of serum immunoglobulins, Biopsy, Acid Fast Bacilli (AFB), Electrolytes assay and comple¬ment levels. The Management and Treatment of immunodeficiency disorders include Antiviral therapy like the such as amantidine and ramantadine which may be life-saving in the management of viral infections, Intravenous or subcutaneous immunoglobulins replacement, Bone marrow transplant, Blood transfusion, Thymus transplants , Gene therapy, Stem cell transplant and vaccines. ]]>
Immunodeficiency refers to failure of immune system to encounter infections by different microbial pathogens such as fungi, bacteria, viruses and protozoan. There are two types of immunodeficiency, Primary immunodeficiency disorder (genetic) and Secondary immunodeficiency disorder (acquired). Primary immunodeficiency disorders (PID) are genetic or inherited disorders which make an individual more susceptible to any pathogenic infections. One in two thousands (2,000) children younger than 18 years are thought to have primary immunodeficiency disorder. Antibody, combined B-cell and T-cell, phagocyte and complement disorders are the most common types. Secondary immunodeficiency disorders (SID) arise due to factors such as malnutrition, fatigue, use of immunosuppressants, chemotherapy, skin damage, pregnancy, aging, and recurrent infections. Laboratory screening test for individuals with immunodeficiency disorders include a complete blood count with differential and measurement of serum immunoglobulins, Biopsy, Acid Fast Bacilli (AFB), Electrolytes assay and comple¬ment levels. The Management and Treatment of immunodeficiency disorders include Antiviral therapy like the such as amantidine and ramantadine which may be life-saving in the management of viral infections, Intravenous or subcutaneous immunoglobulins replacement, Bone marrow transplant, Blood transfusion, Thymus transplants , Gene therapy, Stem cell transplant and vaccines. ]]> Wed, 29 Mar 2017 20:40:40 GMT /slideshow/immunodeficiency-in-haematology/73907371 EbiweniLokoja@slideshare.net(EbiweniLokoja) IMMUNODEFICIENCY IN HAEMATOLOGY EbiweniLokoja Immunodeficiency refers to failure of immune system to encounter infections by different microbial pathogens such as fungi, bacteria, viruses and protozoan. There are two types of immunodeficiency, Primary immunodeficiency disorder (genetic) and Secondary immunodeficiency disorder (acquired). Primary immunodeficiency disorders (PID) are genetic or inherited disorders which make an individual more susceptible to any pathogenic infections. One in two thousands (2,000) children younger than 18 years are thought to have primary immunodeficiency disorder. Antibody, combined B-cell and T-cell, phagocyte and complement disorders are the most common types. Secondary immunodeficiency disorders (SID) arise due to factors such as malnutrition, fatigue, use of immunosuppressants, chemotherapy, skin damage, pregnancy, aging, and recurrent infections. Laboratory screening test for individuals with immunodeficiency disorders include a complete blood count with differential and measurement of serum immunoglobulins, Biopsy, Acid Fast Bacilli (AFB), Electrolytes assay and comple¬ment levels. The Management and Treatment of immunodeficiency disorders include Antiviral therapy like the such as amantidine and ramantadine which may be life-saving in the management of viral infections, Intravenous or subcutaneous immunoglobulins replacement, Bone marrow transplant, Blood transfusion, Thymus transplants , Gene therapy, Stem cell transplant and vaccines. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/jamesebi-170329204041-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Immunodeficiency refers to failure of immune system to encounter infections by different microbial pathogens such as fungi, bacteria, viruses and protozoan. There are two types of immunodeficiency, Primary immunodeficiency disorder (genetic) and Secondary immunodeficiency disorder (acquired). Primary immunodeficiency disorders (PID) are genetic or inherited disorders which make an individual more susceptible to any pathogenic infections. One in two thousands (2,000) children younger than 18 years are thought to have primary immunodeficiency disorder. Antibody, combined B-cell and T-cell, phagocyte and complement disorders are the most common types. Secondary immunodeficiency disorders (SID) arise due to factors such as malnutrition, fatigue, use of immunosuppressants, chemotherapy, skin damage, pregnancy, aging, and recurrent infections. Laboratory screening test for individuals with immunodeficiency disorders include a complete blood count with differential and measurement of serum immunoglobulins, Biopsy, Acid Fast Bacilli (AFB), Electrolytes assay and comple¬ment levels. The Management and Treatment of immunodeficiency disorders include Antiviral therapy like the such as amantidine and ramantadine which may be life-saving in the management of viral infections, Intravenous or subcutaneous immunoglobulins replacement, Bone marrow transplant, Blood transfusion, Thymus transplants , Gene therapy, Stem cell transplant and vaccines.
IMMUNODEFICIENCY IN HAEMATOLOGY from Ebiweni Lokoja
]]> 249 2 https://cdn.slidesharecdn.com/ss_thumbnails/jamesebi-170329204041-thumbnail.jpg?width=120&height=120&fit=bounds presentation Black http://activitystrea.ms/schema/1.0/post http://activitystrea.ms/schema/1.0/posted 0 ALPHA FETO PROTEIN: A BIOMAKER OF SPINA BIFIA /slideshow/alpha-feto-protein-a-biomaker-of-spina-bifia/73907083 sbdntd-170329203616
Alpha feto protein (AFP) is the first α – globulin to appear in human sera during development of the embryo. It contains approximately 4% carbohydrate with molecular mass of approximately 70, 000 Kilo Dalton; AFP is Synthesize primary by the fetal yolk and liver. Spina bifida, which literally means “cleft spine,” is characterized by the incomplete development of the brain, spinal cord, and/or meninges. There are three main types: spina bifida occulta, meningocele, and myelomeningocele. Causes of spina bifida can be either Genetic or multifactorial. Laboratory diagnosis includes Alpha feto protein assay, Amniocentesis and ultrasound. Management of spina bifida includes folic acid intake and surgery. ]]>
Alpha feto protein (AFP) is the first α – globulin to appear in human sera during development of the embryo. It contains approximately 4% carbohydrate with molecular mass of approximately 70, 000 Kilo Dalton; AFP is Synthesize primary by the fetal yolk and liver. Spina bifida, which literally means “cleft spine,” is characterized by the incomplete development of the brain, spinal cord, and/or meninges. There are three main types: spina bifida occulta, meningocele, and myelomeningocele. Causes of spina bifida can be either Genetic or multifactorial. Laboratory diagnosis includes Alpha feto protein assay, Amniocentesis and ultrasound. Management of spina bifida includes folic acid intake and surgery. ]]> Wed, 29 Mar 2017 20:36:16 GMT /slideshow/alpha-feto-protein-a-biomaker-of-spina-bifia/73907083 EbiweniLokoja@slideshare.net(EbiweniLokoja) ALPHA FETO PROTEIN: A BIOMAKER OF SPINA BIFIA EbiweniLokoja Alpha feto protein (AFP) is the first α – globulin to appear in human sera during development of the embryo. It contains approximately 4% carbohydrate with molecular mass of approximately 70, 000 Kilo Dalton; AFP is Synthesize primary by the fetal yolk and liver. Spina bifida, which literally means “cleft spine,” is characterized by the incomplete development of the brain, spinal cord, and/or meninges. There are three main types: spina bifida occulta, meningocele, and myelomeningocele. Causes of spina bifida can be either Genetic or multifactorial. Laboratory diagnosis includes Alpha feto protein assay, Amniocentesis and ultrasound. Management of spina bifida includes folic acid intake and surgery. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/sbdntd-170329203616-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Alpha feto protein (AFP) is the first α – globulin to appear in human sera during development of the embryo. It contains approximately 4% carbohydrate with molecular mass of approximately 70, 000 Kilo Dalton; AFP is Synthesize primary by the fetal yolk and liver. Spina bifida, which literally means “cleft spine,” is characterized by the incomplete development of the brain, spinal cord, and/or meninges. There are three main types: spina bifida occulta, meningocele, and myelomeningocele. Causes of spina bifida can be either Genetic or multifactorial. Laboratory diagnosis includes Alpha feto protein assay, Amniocentesis and ultrasound. Management of spina bifida includes folic acid intake and surgery.
ALPHA FETO PROTEIN: A BIOMAKER OF SPINA BIFIA from Ebiweni Lokoja
]]> 238 2 https://cdn.slidesharecdn.com/ss_thumbnails/sbdntd-170329203616-thumbnail.jpg?width=120&height=120&fit=bounds presentation Black http://activitystrea.ms/schema/1.0/post http://activitystrea.ms/schema/1.0/posted 0 ALCOHOLIC LIVER DISEASE /slideshow/alcoholic-liver-disease-73906715/73906715 ald-170329202845
Alcoholic liver disease (ALD) encompasses a spectrum of injury, ranging from simple steatosis to frank cirrhosis and is the oldest form of liver injury known to mankind. The pathophysiology of ALD is quite complex: encompassing factors related to genetics, gender, ethnicity, consumption patterns and co-morbid conditions. The diagnosis of ALD is based on a combination of features, including history of ‘significant’ alcohol intake, clinical evidence of liver disease, and supporting laboratory abnormalities such as Alanine aminotransferase (ALAT), Aspartate aminotransferase (ASAT), Hepatic imaging, Full blood count and liver biopsy. Treatment and management of alcoholic liver disease are abstinence from alcohol, Liver Transplantation and Therapy for Alcoholic Hepatitis which includes Nutrition Therapy, and Steroids.]]>
Alcoholic liver disease (ALD) encompasses a spectrum of injury, ranging from simple steatosis to frank cirrhosis and is the oldest form of liver injury known to mankind. The pathophysiology of ALD is quite complex: encompassing factors related to genetics, gender, ethnicity, consumption patterns and co-morbid conditions. The diagnosis of ALD is based on a combination of features, including history of ‘significant’ alcohol intake, clinical evidence of liver disease, and supporting laboratory abnormalities such as Alanine aminotransferase (ALAT), Aspartate aminotransferase (ASAT), Hepatic imaging, Full blood count and liver biopsy. Treatment and management of alcoholic liver disease are abstinence from alcohol, Liver Transplantation and Therapy for Alcoholic Hepatitis which includes Nutrition Therapy, and Steroids.]]> Wed, 29 Mar 2017 20:28:45 GMT /slideshow/alcoholic-liver-disease-73906715/73906715 EbiweniLokoja@slideshare.net(EbiweniLokoja) ALCOHOLIC LIVER DISEASE EbiweniLokoja Alcoholic liver disease (ALD) encompasses a spectrum of injury, ranging from simple steatosis to frank cirrhosis and is the oldest form of liver injury known to mankind. The pathophysiology of ALD is quite complex: encompassing factors related to genetics, gender, ethnicity, consumption patterns and co-morbid conditions. The diagnosis of ALD is based on a combination of features, including history of ‘significant’ alcohol intake, clinical evidence of liver disease, and supporting laboratory abnormalities such as Alanine aminotransferase (ALAT), Aspartate aminotransferase (ASAT), Hepatic imaging, Full blood count and liver biopsy. Treatment and management of alcoholic liver disease are abstinence from alcohol, Liver Transplantation and Therapy for Alcoholic Hepatitis which includes Nutrition Therapy, and Steroids. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ald-170329202845-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Alcoholic liver disease (ALD) encompasses a spectrum of injury, ranging from simple steatosis to frank cirrhosis and is the oldest form of liver injury known to mankind. The pathophysiology of ALD is quite complex: encompassing factors related to genetics, gender, ethnicity, consumption patterns and co-morbid conditions. The diagnosis of ALD is based on a combination of features, including history of ‘significant’ alcohol intake, clinical evidence of liver disease, and supporting laboratory abnormalities such as Alanine aminotransferase (ALAT), Aspartate aminotransferase (ASAT), Hepatic imaging, Full blood count and liver biopsy. Treatment and management of alcoholic liver disease are abstinence from alcohol, Liver Transplantation and Therapy for Alcoholic Hepatitis which includes Nutrition Therapy, and Steroids.
ALCOHOLIC LIVER DISEASE from Ebiweni Lokoja
]]> 2013 2 https://cdn.slidesharecdn.com/ss_thumbnails/ald-170329202845-thumbnail.jpg?width=120&height=120&fit=bounds presentation Black http://activitystrea.ms/schema/1.0/post http://activitystrea.ms/schema/1.0/posted 0 https://public.slidesharecdn.com/v2/images/profile-picture.png https://cdn.slidesharecdn.com/ss_thumbnails/jamesebi-170329204041-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/immunodeficiency-in-haematology/73907371 IMMUNODEFICIENCY IN HA... https://cdn.slidesharecdn.com/ss_thumbnails/sbdntd-170329203616-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/alpha-feto-protein-a-biomaker-of-spina-bifia/73907083 ALPHA FETO PROTEIN: A ... https://cdn.slidesharecdn.com/ss_thumbnails/ald-170329202845-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/alcoholic-liver-disease-73906715/73906715 ALCOHOLIC LIVER DISEASE