Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Other Names for this Disease
- Attenuated congenital adrenal hyperplasia
- Non classic congenital adrenal hyperplasia
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congenital adrenal hyperplasia (CAH). Individuals with CAH are usually diagnosed as newborns, whereas those with LOCAH are diagnosed later in life. In females, symptoms may include excessive hair growth, absent periods, infertility, hair loss (androgenic alopecia), masculinized genitalia, and acne. Many of these symptoms overlap with other disorders, including polycystic ovarian syndrome. Males with LOCAH may have early beard growth, an enlarged penis with small testes, a low sperm count, and short stature. Late-onset congenital adrenal hyperplasia (LOCAH) is a variation of a genetic disorder known as
Last updated: 2/15/2010
- Non-classical Adrenal Hyperplasia . CARES Foundation Web site. http://www.caresfoundation.org/ProductCart/pc/ncah_late_onset_cah.html. Accessed 11/10/2008.
- Genetics Home Reference (GHR) contains information on Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. This website is maintained by the National Library of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Click on the link to view a sample search on this topic.
- Section on Endocrinology and Committee on Genetics. Technical Report: Congenital Adrenal Hyperplasia. Pediatrics; 2000;106(6):1511-1518.