skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: PPM-X: A new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28

Journal Article · · American Journal of Human Genetics
OSTI ID:446927
; ;  [1]
  1. Univ. of Newcastle upon Tyne (United Kingdom); and others

We report a three-generation family manifesting a previously undescribed X-linked mental retardation syndrome. Four of the six moderately retarded males have had episodes of manic-depressive psychosis. The phenotype also includes pyramidal signs, Parkinsonian features, and macroorchidism, but there are no characteristic dysmorphic facial features. Affected males do not show fragile sites at distal Xq on cytogenetic analysis, nor do they have expansions of the CGG repeats at the FRAXA, FRAXE, or FRAXF loci. Linkage analyses were undertaken, and a maximal LOD score of 3.311 at {theta} = .0 was observed with the microsatellite marker DXS1123 in Xq28. A recombination was detected in one of the affected males with DXS1691 (Xq28), which gives the proximal boundary of the localization. No distal recombination has been detected at any of the loci tested. 31 refs., 2 figs., 2 tabs.

OSTI ID:
446927
Journal Information:
American Journal of Human Genetics, Vol. 58, Issue 6; Other Information: PBD: Jun 1996
Country of Publication:
United States
Language:
English

Similar Records

Cloning and characterization of an unstable CGG repeat related to a fragile site in Xq28: A FRAXF candidate
Journal Article · Thu Sep 01 00:00:00 EDT 1994 · American Journal of Human Genetics · OSTI ID:446927

FRAXE expansion is not a common etiological factor among developmentally delayed males
Journal Article · Sat Jul 01 00:00:00 EDT 1995 · American Journal of Human Genetics · OSTI ID:446927

Triplet repeat expansion at the FRAXE locus and x-linked mild mental handicap
Journal Article · Fri Jul 01 00:00:00 EDT 1994 · American Journal of Human Genetics; (United States) · OSTI ID:446927