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Late-onset congenital adrenal hyperplasia
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 Late-onset congenital adrenal hyperplasia. This website is maintained by the National Library of Medicine.
In Depth Information
- The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Late-onset congenital adrenal hyperplasia. Click on the link to view a sample search on this topic.
Selected Full-Text Journal Articles
- Section on Endocrinology and Committee on Genetics. Technical Report: Congenital Adrenal Hyperplasia. Pediatrics; 2000;106(6):1511-1518.