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A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

Lookup NU author(s): Professor Susan Lindsay, Dr Miranda Splitt, Professor Sir John Burn

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Abstract

We report here the genetic cause of the X-linked syndrome of psychosis, pyramidal signs, and macro-orchidism (PPM-X) in a three-generation family manifesting the disorder as a mutation in the methyl-CpG binding-protein 2 (MECP2) gene in Xq28. The A140V mutation was found in all affected males and all carrier females in the family. To date, descriptions have been published of two patients with independent familial mental retardation (MR) and two patients with sporadic MR who harbor this specific mutation in the MECP2 gene. This strongly suggests that A140V is a hot spot of mutation resulting in moderate to severe MR in males. A simple and reliable PCR approach has been developed for detection of the hot spot A140V mutation to prescreen any other unexplained cases of MR before further extensive mutation analyses.


Publication metadata

Author(s): Klauck SM, Lindsay S, Beyer KS, Splitt M, Burn J, Poustka A

Publication type: Article

Publication status: Published

Journal: American Journal of Human Genetics

Year: 2002

Volume: 70

Issue: 4

Pages: 1034-1037

ISSN (print): 0002-9297

ISSN (electronic): 1537-6605

Publisher: Cell Press

URL: http://dx.doi.org/10.1086/339553

DOI: 10.1086/339553


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