| Literature DB >> 23769969 |
Yoo-Mi Kim1, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Han Hyuk Lim, Han-Wook Yoo.
Abstract
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder. Ornithine transcarbamylase (OTC) deficiency is the most common urea cycle disorder and demonstrates X-linked inheritance. In female OTC deficiency, phenotypes are variable according to X-inactivation patterns. These disorders develop separately, and their co-morbidity is extremely rare. We report one girl with CAH showing recurrent hyperammonemia and hepatitis after 2 years-of-age due to additional OTC deficiency.Entities:
Keywords: 17-Hydroxyprogesterone; 17-OHP; 21-Hydroxylase deficient congenital adrenal hyperplasia; CAH; Co-morbidity; OTC; Ornithine transcarbamylase deficiency; Urea cycle disorder; congenital adrenal hyperplasia; ornithine transcarbamylase
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Year: 2013 PMID: 23769969 DOI: 10.1016/j.gene.2013.03.096
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688