Literature DB >> 22887700

Phenotype in novel Xp duplication.

Manju Salaria1, Trent Burgess, Stella Setyapranata, Ingrid Winship.   

Abstract

A novel duplication of Xp is described. A 20-year-old man had minor anomalies ichthyosis, congenital heart defect, varicose veins, and hypogonadotropic hypogonadism. He had an interstitial duplication of approximately 2.8 Mb from chromosome region Xp22.31p22.2. His similarly affected brother and asymptomatic mother were shown to carry the same duplication. Knowledge about this duplication and its resultant phenotype will add to our understanding of the role of X chromosome duplications.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22887700     DOI: 10.1002/ajmg.a.35538

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


  2 in total

1.  Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features.

Authors:  Carla Lintas; Chiara Picinelli; Ignazio S Piras; Roberto Sacco; Stefano Gabriele; Magda Verdecchia; Antonio M Persico
Journal:  Mol Syndromol       Date:  2016-01-12

2.  A Rare Novel Copy Number Variation of Xp22.33-p11.22 Duplication is Associated with Congenital Heart Defects.

Authors:  Juan Zhang; Qing-Qing Wu; Li Wang; Li-Juan Sun
Journal:  Chin Med J (Engl)       Date:  2015-10-20       Impact factor: 2.628

  2 in total

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