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keywords > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Adrenal Hyperplasia, Congenital
Ambiguous genitalia in neonates: a 4-year prospective study in a localized area.
The case for newborn screening for congenital adrenal hyperplasia in Australia.
Rarer syndromes characterized by hypogonadotropic hypogonadism.
Sexual precocity in a 4 year old boy.
Quantitation of 17-OH-progesterone (OHPG) for diagnosis of congenital adrenal hyperplasia (CAH).
Refractory acne and 21-hydroxylase deficiency in a selected group of female patients.
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency - management in adults.
Giant macroorchidism in congenital adrenal hyperplasia.
The cost of non-compliance in congenital adrenal hyperplasia.
Female children with ambiguous genitalia in awareness-poor subregion.