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Endocrinology MCQ Answer 035
Answer D
Heterosexual precocity (virilization in girls, feminization in boys)
- ovarian tumours
- adrenal tumours
- congenital adrenal hyperplasia (21 OH deficiency)
- congenital adrenal hyperplasia
- 21 hydroxylase deficiency (most common)
→ pseudohermaphroditism (female with virilized external genitals)
→ fused labia, large clitoris
→ ↑ progesterone, ↑ 17-OH progesterone, ↑ androgen
→ impaired aldosterone secretion (↓Na, ↑K)
- 11 hydroxylase deficiency (rare)
- virilization + salt retention (mineralocorticoid activity)
- androgen insensitivity syndrome (testicular feminization)
- 46,XY genotype with ♀ phenotype:
- defective androgen receptor
- blind end vagina, testes are present (must be removed at puberty to prevent cancer)
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