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Male pseudohermaphroditism secondary to 5α-reductase deficiency—A model for the role of androgens in both the development of the male phenotype and the evolution of a male gender identity
(Journal of Steroid Biochemistry, 1979)
Male pseudohermaphroditism secondary to 5α-reductase deficiency is reviewed. At birth, the affected males (46 XY) have a clitoral-like phallus, bifid scrotum and urogenital sinus with the testes in the inguinal canals or ...
Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases — a new variant of congenital adrenal hyperplasia
(New England Journal of Medicine, 1985-11-07)
A six-month-old 46,XY infant with a female phenotype and ambiguous genitalia was evaluated for male pseudohermaphroditism. The principal findings were (1) low basal plasma levels of all measured C19 steroids and their ...
Decreased Urinary C19 and C21 Steroid 5α-Metabolites in Parents of Male Pseudohermaphrodites with 5α- Reductase Deficiency: Detection of Carriers
(The Journal of Clinical Endocrinology & Metabolism, 1985-05-01)
The urinary 5β/5α ring A-reduced metabolites of C19 and C12 steroids from obligate carrier parents of male) pseudohermaphrodites with 5a-reductase deficiency were analyzed by gas chromatography. Etiocholanolone/androsterone, ...