Literature DB >> 25463316

Two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disability.

Bertrand Isidor1, Albert David2.   

Abstract

Here, we report two unrelated girls with prenatal onset short stature, short neck, cervical vertebral anomalies, Sprengel deformity, and mild intellectual disability. The association of these features first suggested a syndromic form of Klippel-Feil anomaly. We therefore analyzed the three known disease causing genes and the candidate gene PAX1. However, direct sequencing of GDF6, GDF3, PAX1, and MEOX1 failed to identify any mutation. To our knowledge, the phenotype we report has not been described previously, leading us to speculate that this condition may represent a new syndrome.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Intellectual disability; Klippel-Feil syndrome; Short stature; Sprengel deformity

Mesh:

Substances:

Year:  2014        PMID: 25463316     DOI: 10.1016/j.ejmg.2014.11.001

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  1 in total

1.  A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel's deformity.

Authors:  Shuai Guo; Xue-Feng Fan; Jie-Yuan Jin; Liang-Liang Fan; Lei Zeng; Zheng-Bing Zhou; Rong Xiang; Ju-Yu Tang
Journal:  Mol Cytogenet       Date:  2018-01-24       Impact factor: 2.009

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.