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CRI-DU-Chat Syndrome - Principles of Inheritance and Variation - Class 12 BiologyRelated Documents
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Hydrocephalus obesity hypogonadism Disease. Hydrocephalus obesity hypogonadism Title Other Names: Congenital hydrocephalus oligophrenia dwarfism centripetal obesity and hypogonadism Categories: Congenital and Genetic Diseases; Endocrine, : DefinitionThis syndrome is characterized by the association of congenital hydrocephaluscentripetal obesityhypogonadismintellectual deficit and short stature.
EpidemiologyIt has been described in two males Obesity due to congenital leptin deficiency Disease. Diagnostic methodsFamily history, severe hyperphagia and early-onset obesity may lead to suspicion of a monogenic obesity syndrome. The diagnosis of congenital leptin deficiency can be confirmed by Alopecia epilepsy oligophrenia syndrome of Moynahan Disease. For most diseases, symptoms will vary from, Alopecia epilepsy oligophrenia syndrome of Moynahan Title Other Names: Moynahan alopecia syndrome; Moynahan syndrome; Alopecia-epilepsy-intellectual disability fri, Moynahan type Categories Lenz Majewski hyperostotic dwarfism Disease.]
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