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Genomics. 1993 Nov;18(2):444-5.

X-linked ocular albinism and sensorineural deafness: linkage to Xp22.3.

Author information

1
Department of Human Genetics, University of Cape Town Medical School, South Africa.

Abstract

X-linked ocular albinism with late-onset sensorineural deafness (OASD) is an autonomous disorder that poses significant clinical problems, causing affected individuals to be blind and deaf by early middle age. Classical X-linked ocular albinism (without deafness; OA1) has recently been linked to markers in the Xp22.2-Xp22.3 region of the human genome. In the present report, a large South African family with OASD was investigated at the molecular level and tight linkage was found to the DXS452 locus at Xp22.3 using 25 informative meioses, with a maximum lod score of 7.1 at a recombination fraction of 0.00. These findings suggest that OA1 and OASD are allelic variants or that they may be due to contiguous gene defects.

PMID:
8288253
DOI:
10.1006/geno.1993.1495
[Indexed for MEDLINE]

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