Ethical aspects of gender assignment in ambiguous genitalia - congenital adrenal hyperplasia: a case report
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder commonly caused by mutation of the CYP21A2 gene, resulting in deficiency of an enzyme required for cortisol synthesis in the adrenal cortex. In 90-95% of cases, the deficient enzyme is 21-hydroxylase (21-OH), with an incidence r...
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| Autores principales: | , , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Indonesian Pediatric Society Publishing House
2021
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/9dac2396569c420187fcad545c89886f |
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