Literature DB >> 12673656

Stocco dos Santos X-linked mental retardation syndrome: clinical elucidation and localization to Xp11.3-Xq21.3.

Rita C Stocco dos Santos1, Nelson H C Castro, A Lillia Holmes, Willy Beçak, Darci Tackels-Horne, Charles J Lindsey, Herbert A Lubs, Roger E Stevenson, Charles E Schwartz.   

Abstract

Mental retardation (MR) affects an estimated 2-3% of the population. A considerable fraction of mental retardation is due to X-linked genes. Of these genes, about 136 are responsible for syndromic X-linked MR (XLMR). One such XLMR syndrome, Stocco dos Santos, was first described in 1991. This family was re-visited, which allowed further delineation of the clinical phenotype. Additionally, linkage analysis was conducted, which resulted in the localization of this XLMR syndrome to the pericentric region, Xp11.3 to Xq21.1, with a maximum LOD score of 3.14 at loci AR and DXS983. Copyright 2003 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12673656     DOI: 10.1002/ajmg.a.20021

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


  6 in total

1.  Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.

Authors:  Olivier Hagens; Aline Dubos; Fatima Abidi; Gotthold Barbi; Laura Van Zutven; Maria Hoeltzenbein; Niels Tommerup; Claude Moraine; Jean-Pierre Fryns; Jamel Chelly; Hans van Bokhoven; Jozef Gécz; Hélène Dollfus; Hans-Hilger Ropers; Charles E Schwartz; Rita de Cassia Stocco Dos Santos; Vera Kalscheuer; André Hanauer
Journal:  Hum Genet       Date:  2005-10-26       Impact factor: 4.132

2.  A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical Spectrum.

Authors:  Pinar Arican; Dilek Cavusoglu; Pinar Gencpinar; Berk Ozyilmaz; Taha Resid Ozdemir; Nihal Olgac Dundar
Journal:  J Pediatr Genet       Date:  2017-12-18

3.  The genetic basis of non-syndromic intellectual disability: a review.

Authors:  Liana Kaufman; Muhammad Ayub; John B Vincent
Journal:  J Neurodev Disord       Date:  2010-07-29       Impact factor: 4.025

4.  Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability.

Authors:  Christina Grau; Molly Starkovich; Mahshid S Azamian; Fan Xia; Sau Wai Cheung; Patricia Evans; Alex Henderson; Seema R Lalani; Daryl A Scott
Journal:  PLoS One       Date:  2017-04-17       Impact factor: 3.240

5.  Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report.

Authors:  Magdalena Danyel; Eun Kyung Suk; Vera Raile; Jutta Gellermann; Alexej Knaus; Denise Horn
Journal:  BMC Med Genomics       Date:  2019-01-10       Impact factor: 3.063

6.  NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment.

Authors:  Jillian P Casey; Svein I Støve; Catherine McGorrian; Joseph Galvin; Marina Blenski; Aimee Dunne; Sean Ennis; Francesca Brett; Mary D King; Thomas Arnesen; Sally Ann Lynch
Journal:  Sci Rep       Date:  2015-11-02       Impact factor: 4.379

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.