Literature DB >> 22786695

A family with radio-ulnar synostosis, scoliosis, and thick vermilion of lips: a novel syndrome or variant of Giuffrè-Tsukahara syndrome?

Yimin Zhu1, Ke Jin, Haibo Mei, Liping Li, Zheng Liu, Yongjia Yang, Jingsong Tang, Xielin He, Rui Zhao, Xinyu He.   

Abstract

We report on a three-generation Chinese family presenting with a recognizable condition consisting of radio-ulnar synostosis, short stature, scoliosis, distinctive craniofacial features (thick vermilion to the lips, prominent eyes, and flat malar region), and a shortened and thickened femur neck. The inheritance of the trait was presumably autosomal dominant. The lack of microcephaly in the family suggested a variant of Giuffè-Tsukahara syndrome but could represent variability
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22786695     DOI: 10.1002/ajmg.a.35478

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


  2 in total

1.  BMPR1B mutation causes Pierre Robin sequence.

Authors:  Yongjia Yang; Jianying Yuan; Xu Yao; Rong Zhang; Hui Yang; Rui Zhao; Jihong Guo; Ke Jin; Haibo Mei; Yongqi Luo; Liu Zhao; Ming Tu; Yimin Zhu
Journal:  Oncotarget       Date:  2017-04-18

2.  Mutant B3GALT6 in a Multiplex Family: A Dominant Variant Co-Segregated With Moderate Malformations.

Authors:  Fang Shen; Yongjia Yang; Yu Zheng; Ming Tu; Liu Zhao; Zhenqing Luo; Yuyan Fu; Yimin Zhu
Journal:  Front Genet       Date:  2022-06-06       Impact factor: 4.772

  2 in total

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