| Literature DB >> 24293885 |
Alka Kriplani1, Amol Lunkad, Nutan Agarwal, Bindu Kulshreshtha, C Aminni Ariachery.
Abstract
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders characterized by enzyme defects in adrenal steroidogenic pathways. CAH due to 21-hydroxylase deficiency accounts for 95 % of cases. This case was diagnosed to have simple virilizing type of CAH and started on dexamethasone, and underwent genitoplasty and clitoroplasty at 25 years of age, then was married 3 years after surgery and conceived spontaneously 2 years after marriage, to deliver a healthy male baby. Thus, proper diagnosis and treatment with steroids and genitoplasty can give females with CAH a normal sexual, normal menstrual, and reproductive function.Entities:
Year: 2013 PMID: 24293885 PMCID: PMC3632694 DOI: 10.1007/s13224-013-0387-1
Source DB: PubMed Journal: J Obstet Gynaecol India ISSN: 0975-6434