Opis choroby * EnglishPolish Pobierz sekcję do PDF Definicja A rare form of congenital adrenal hyperplasia (CAH) due to 3-beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency and characterized by salt-wasting and non-salt wasting CAH with a wide variety of symptoms, including glucocorticoid and mineralocorticoid deficiencies in both sexes. Salt wasting can lead to dehydration and hypotension in the first few weeks of life. Affected males had undervirilization manifesting as a micropenis to severe perineoscrotal hypospadias. Females show normal or mildly virilized external genitalia (mild clitoromegaly, labial fusion) due to dehydroepiandrosterone (DHEA) accumulation and conversion to androgens by the normal HSD3B1. Dane Klasyfikacja Choroba Synonimy CAH due to 3-beta-hydroxysteroid dehydrogenase deficiency CAH z powodu niedoboru dehydrogenazy 3-beta-hydroksysteroidowej Kod ORPHA 90791 Kod OMIM 201810 Kod ICD10 E25.0 Kod ICD11 5A71.01 *Źródło Rozszerzony opis choroby Pobierz sekcję do PDF Brak opisu rozszerzonego dla tej choroby. Opracowanie w toku. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl