Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: Redefining a clinical entity

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Item Type:	Article
Title:	Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: Redefining a clinical entity
Creators Name:	Horn, D., Krebsova, A., Kunze, J. and Reis, A.
Abstract:	A syndrome of microcephaly, progressive postnatal growth deficiency, and mental retardation was observed in two brothers and their cousin from a multiply consanguineous kindred of Lebanese descent. Hypotonia, chorioretinal dystrophy, and myopia were also identified. The severity of the condition varied among the closely related patients. Because of absence of a distinctive facial appearance, the degree of mental retardation, and short stature, the initially considered clinical diagnosis of Cohen syndrome was withdrawn and a novel genetic entity was assumed. Homozygosity mapping in this family assigned the gene to a 26.8-cM region on the chromosome band 8q21.3 -22.1, between the microsatellites at D8S270 and D8S514. The maximum two-point LOD score was found for marker at D8S267 (Z(max)=3.237 at O(max)=0.00). Intriguingly enough, the identified gene region overlaps the refined gene region for Cohen syndrome (COH1) [Kolehmainen et al., 1997: Euro J Hum Genet 5:206213]. This fact encourages the hypothesis that the described kindred segregates for a variant of Cohen syndrome and suggests a redefinition of its phenotype.
Keywords:	Chorioretinal Dystrophy, Heterogeneity, Hypotonia, Mirhosseini-Holmes-Walton Syndrome
Source:	American Journal of Medical Genetics
ISSN:	0148-7299
Publisher:	Wiley-Liss
Volume:	92
Number:	4
Page Range:	285-292
Date:	5 June 2000
Official Publication:	https://doi.org/10.1002/(SICI)1096-8628(20000605)92:4<285::AID-AJMG13>3.0.CO;2-D
PubMed:	View item in PubMed

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