Literature DB >> 24551980

A case of dup(3q) syndrome.

A Koç1, A Yilmaz Ekmekci2, O Ozer3.   

Abstract

Duplication of 3q is an extremely rare disorder characterized by "intellectual disability, deficiency of growth, broad nasal root and hypertrichosis". Although it is generally accepted that the duplication of the 3q25-qter region corresponds with a characteristic face, there is a debate about the critical region. In this report, we present a case with dup(3q) syndrome with 46,XY,der(7)ins(7;3)(p13; q22.1q26.31) karyotype and discuss the clinical findings.

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Year:  2013        PMID: 24551980

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  1 in total

1.  Rare de novo inversion-duplication case with pure 3qter duplication syndrome including an overlap of the dup(3q) critical region: A case report.

Authors:  George Imataka; Yoshiyuki Watabe; Sayuri Kajitani; Shun Watanabe; Junko Ichikawa; Fabrizio Drago; Hiroshi Suzumura; Shigemi Yoshihara
Journal:  Exp Ther Med       Date:  2017-05-03       Impact factor: 2.447

  1 in total

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