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...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article PeerReviewed |
| Language: | English English English English |
| Published: |
Indonesian Pediatric Society
2021
|
| Subjects: | |
| Online Access: | https://repository.unair.ac.id/126446/1/9%20-%20Artikel.pdf https://repository.unair.ac.id/126446/2/9%20-%20Korespondensi.pdf https://repository.unair.ac.id/126446/3/9%20-%20Kualitas%20Karil.pdf https://repository.unair.ac.id/126446/4/9%20-%20Turnitin.pdf https://repository.unair.ac.id/126446/ https://www.paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2376 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Institution: | Universitas Airlangga |
| Language: | English English English English |