Aldred syndrome
| Aldred syndrome | |
|---|---|
| Other names | Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion |
| Symptoms | Intellectual disability Retinitis pigmentosa |
| Usual onset | Congenital |
| Causes | Deletion on X-chromosome p11.3 |
Aldred syndrome is an X-linked recessive genetic disorder. It is mainly characterized by a form of intellectual disability and retinitis pigmentosa. The syndrome was first described by geneticist Micheala Aldred in 1994.[1]
Cause
[edit]Aldred syndrome is caused by a deletion on the p11.3 area of the X-chromosome.[2]
References
[edit]- ^ Aldred, M. A.; Dry, K. L.; Knight-Jones, E. B.; Hardwick, L. J.; Teague, P. W.; Lester, D. H.; Brown, J.; Spowart, G.; Carothers, A. D. (November 1994). "Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa". American Journal of Human Genetics. 55 (5): 916–922. ISSN 0002-9297. PMC 1918325. PMID 7977353.
- ^ "OMIM Entry - # 300578 - CHROMOSOME Xp11.3 DELETION SYNDROME". omim.org. Retrieved 2019-04-28.
External links
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