Literature DB >> 9674901

Duplication 6q22-->qter: definition of the phenotype.

B A Conrad1, R R Higgins, M E Pierpont.   

Abstract

We report on a girl with duplication of 6q22.32 --> qter and microcephaly, frontal bossing, facial anomalies, and webbed neck. She has congenital heart disease, renal hypoplasia, and hearing loss along with severe developmental delay. Published reports of seven other patients are reviewed and compared. The most frequent anomalies include microcephaly, abnormal face, webbed neck, congenital heart disease, limb contractures, and developmental delay.

Entities:  

Mesh:

Year:  1998        PMID: 9674901     DOI: 10.1002/(sici)1096-8628(19980630)78:2<123::aid-ajmg5>3.0.co;2-p

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  A Chinese multicenter retrospective study of isolated increased nuchal translucency associated chromosome anomaly and prenatal diagnostic suggestions.

Authors:  Hua Jin; Juan Wang; Guoying Zhang; Hongyan Jiao; Jiansheng Zhu; Zhimin Li; Chen Chen; XuanPing Zhang; Huan Huang; JiaYin Wang
Journal:  Sci Rep       Date:  2021-03-10       Impact factor: 4.379

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.