We describe a large family with nonspecific X-linked mental retardation (MRX 47). An X-linked recessive transmission is suggested by the inheritance from the mothers in two generations of a moderate to severe form of mental retardation in six males, without any specific clinical findings. Two point
Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26
β Scribed by Caspari, Reiner ;Uhlhaas, Siegfried ;Friedl, Waltraut ;Knapp, Michael ;Propping, Peter
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 216 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0148-7299
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β¦ Synopsis
Nonspecific X-linked mental retardation is a heterogeneous condition consisting of nonsyndromal mental retardation in males. It is caused by mutation in one of several genes on the X chromosome (MRX genes). Here we report on the localization of a presumptive MRX gene to chromosomal region Xq24-q26 in a German family with nonspecific X-linked mental retardation (MRX 75, HUGO Human Gene Nomenclature Committee). Two point linkage analysis with 23 informative markers gave a lod score of 2.53 at theta = 0 for markers DXS425, DXS1254, DXS1114, and HPRT.
π SIMILAR VOLUMES
## Abstract Isolated mental retardation is clinically and genetically heterogenous and may be inherited in an autosomal dominant, autosomal recessive, or Xβlinked manner. We report here a linkage analysis in a large family including 15 members, 6 of whom presenting Xβlinked nonβsyndromic mental ret
A large family with non-specific X-linked mental retardation (MRX) was first described in 1991 [Glass et al., 19911, with a suggestion of linkage to Xq26-27. The maximum lod score was 1.60 (0 = 0.10) with the F9 locus. The localisation of this MRX gene has now been established by linkage to microsat
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