Fragile X syndrome: Causes, Symptoms, Diagnosis and Treatment
Fragile X syndrome (FXS): Fragile X syndrome is also known as marker X syndrome or Martin-Bell syndrome. It is one of the genetic disorders that […]
Fragile X syndrome (FXS): Fragile X syndrome is also known as marker X syndrome or Martin-Bell syndrome. It is one of the genetic disorders that […]
Visceral leishmaniasis (VL) or Kala-azar: Visceral Leishmaniasis (VL) also known as kala-azar or black fever or dum-dum fever, is the most severe form of leishmaniasis. […]
Hookworms: Hookworms are parasitic nematode that lives in the small intestine of mammalian host such as dog, cat or humans. They are characterized by their […]
Specimens: It includes nasal mucosa, skin lesions, ear lobules. Occasionally, lymph nodes and affected nerves. Method of collecting of skin smears: Slit and scrap method: […]
Leprosy: Hansen’s disease (leprosy) is a chronic granulomatous disease of humans primarily involving the skin, peripheral nerves and nasal mucosa but capable of affecting any […]
Marfan syndrome: Marfan syndrome is one of the genetic disorders i.e. the child inherits from their parents. It is a condition that affects the connective […]
Cystic fibrosis: Cystic fibrosis (CF) is one of the genetic diseases i.e. it can be inherited to offspring. It is the condition where the mucus […]
Thalassemia Thalassemia is a common term for a group of inheritable, genetic diseases characterized by reduced levels of Hemoglobin, low RBCs production and anemia. There […]
β-thalassemia β-thalassemia is also termed as erythroblastic anaemia, β-type microcytemia, or Mediterranean anaemia. The term thalassemia was coined by George Whipple and William Bradford, in […]
Huntington’s disease: It is also known as Huntington chorea It is one of rare and fatal diseases that accounts for the gradual breakdown of brain […]
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