Categories
Crandall syndrome
Topic: Medicine
From HandWiki - Reading time: 1 min
| Crandall syndrome | |
|---|---|
| Other names | Alopecia-deafness-hypogonadism syndrome |
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| Crandall syndrome is inherited in an autosomal recessive manner | |
Crandall syndrome is a very rare congenital disorder characterised by progressive sensorineural hearing loss, hair loss associated with pili torti, and hypogonadism demonstrated through low levels of luteinising hormone and growth hormone. It is thought to be an autosomal recessive disorder closely related to Björnstad syndrome which presents similarly but without hypogonadism.[1]
The condition was first reported by B. F. Crandall in 1973.[2]
References
- ↑ "Orphanet: Crandall syndrome". http://www.orpha.net/consor4.01/www/cgi-bin/OC_Exp.php?lng=EN&Expert=202.
- ↑ Crandall BF, Samec L, Sparkes RS, Wright SW (1973). "A familial syndrome of deafness, alopecia, and hypogonadism". J Pediatr 82 (3): 461–5. doi:10.1016/s0022-3476(73)80121-0. PMID 4698933.
External links
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Licensed under CC BY-SA 3.0 | Source: https://handwiki.org/wiki/Medicine:Crandall_syndrome1 views | ↧ Download this article as ZWI file
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