Literature DB >> 12605440

Shashi XLMR syndrome: report of a second family.

Nelson H C Castro1, Rita C Stocco dos Santos, Retecher Nelson, Willy Beçak, Bernhard Hane, Charles J Lindsey, Herbert A Lubs, Roger E Stevenson, Charles E Schwartz.   

Abstract

This report describes a family with mental retardation in two brothers. The pedigree is consistent with either X-linked mental retardation or autosomal recessive inheritance. The clinical features consist of coarse face, prominent lower lip, large testes, and obesity. This same constellation of findings was observed in a family with X-linked mental retardation (XLMR) reported by Shashi et al. [2000: Am J Hum Genet 66:469-479]. Furthermore, haplotype analysis was consistent with localization of the Shashi XLMR syndrome in Xq26-q27. Thus, the family likely represents a second occurrence of the Shashi XLMR syndrome. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12605440     DOI: 10.1002/ajmg.a.10888

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  IGSF1 deficiency syndrome: A newly uncovered endocrinopathy.

Authors:  Sjoerd D Joustra; A S Paul van Trotsenburg; Yu Sun; Monique Losekoot; Daniel J Bernard; Nienke R Biermasz; Wilma Oostdijk; Jan M Wit
Journal:  Rare Dis       Date:  2013-05-02

2.  Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26.

Authors:  Maribeth A Lazzaro; Matthew A M Todd; Paul Lavigne; Dominic Vallee; Adriana De Maria; David J Picketts
Journal:  BMC Med Genet       Date:  2008-02-26       Impact factor: 2.103

  2 in total

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