Abdallat Davis Farrage syndrome
Wikipedia on Answers.com:
Top
Abdallat Davis Farrage syndrome
 |
This article may be confusing or unclear to readers. Please help clarify the article; suggestions may be found on the talk page. (July 2008) |
 |
This article needs attention from an expert on the subject. See the talk page for details. WikiProject Medicine or the Medicine Portal may be able to help recruit an expert. (July 2008) |
| Abdallat Davis Farrage syndrome | |
|---|---|
| Classification and external resources | |
| OMIM | 270750 |
Abdallat Davis Farrage syndrome is a phakomatosis consisting of disordered skin and hair pigmentation, progressive spastic paraparesis and peripheral neuropathy. It is a type of neurocutaneous syndromes, called Abdallat type.
It was characterized in 1980 by Adnan Abdallat, a Jordanian doctor.[1]
The syndrome is thought to be inherited as an autosomal recessive genetic trait.
Symptoms
- Albinism (hair)
- Irregular decreased skin pigmentation
- Excessive freckling
- Insensitivity to pain
- Paraparesis/quadraparesis
References
- ^ Abdallat A, Davis SM, Farrage J, McDonald WI (1980). "Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome". J Neurol Neurosurg Psychiatry 43 (11): 962–6. doi:10.1136/jnnp.43.11.962. PMC 490745. PMID 7441281. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=490745.
External links
|
||||||||||||||
 |
This genetic disorder article is a stub. You can help Wikipedia by expanding it. |
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
Post a question - any question - to the WikiAnswers community:
Copyrights:
Wikipedia on Answers.com
This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article Abdallat Davis Farrage syndrome.
Read more