Galactosemia

An autosomal recessive inherited metabolic disorder caused by mutations in the GALE, GALK1, and GALT genes. It is characterized by deficiency of the enzymes responsible for the metabolism of galactose. Signs and symptoms include intellectual disability, hepatomegaly, hepatic failure, and renal failure.

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WHO"s CLASSIFICATION OF ANOVULATION

TYPES OF ANOVULATION & TREATMENT: WHO CLASSIFICATION. TYPE I : Hypogonadotropic - Reduced FSH. Hypoestrogenic - ...See More

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So first type is stress induced amenorrhea, second is PCOS,third is ovarian failure and fourth is prolactin induced amenorrhea.


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NEONATAL CHOLESTASIS 1) Bile duct obstruction Extrahepatic biliary atresia 2) Neonatal infection Cytomegalovirus Bacterial sepsis Urinary tract infection Syphilis 3) Toxic Drugs Parenteral nutrition 4) Genetic disorders Tyrosinemia Ne...See More

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Prolonged conjugated hyperbilirubinemia in a neonate is termed as neonatal cholestasis


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