| Literature DB >> 10398233 |
F Abidi1, B D Hall, R G Cadle, G L Feldman, H A Lubs, L V Ouzts, J F Arena, R E Stevenson, C E Schwartz.
Abstract
Clinical and molecular studies are reported on a family with X-linked mental retardation (XLMR) in which there are eight affected males in three generations. Although the males have somatic manifestations, these are variable and in most cases do not allow clear distinction of affected and unaffected males. Affected males are shorter and have a smaller head circumference. Several also have a sloping forehead (5/8), hearing loss (3/8), cupped ears (2/8), and small testes (4/6). An LOD score of 4.41 with zero recombination was obtained at locus DXS1166 in Xq13.2. This family highlights the difficulty in classifying XLMR conditions as either nonsyndromic or syndromic because of the variable somatic manifestations observed in the affected males. Copyright 1999 Wiley-Liss, Inc.Entities:
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Year: 1999 PMID: 10398233 DOI: 10.1002/(sici)1096-8628(19990730)85:3<223::aid-ajmg8>3.0.co;2-r
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299