Literature DB >> 11339372

The 22q11.2 deletion: from diversity to a single gene theory.

H P De Decker1, J B Lawrenson.   

Abstract

The 22q11 deletion syndromes are a group of conditions in which a characteristic spectrum of congenital cardiac defects may be associated with a wide range of noncardiological congenital anomalies. These syndromes are all linked by a deletion in the long arm of chromosome 22. Although it is a large deletion, containing many genes, recent advances have led to the belief that the etiology of the diverse abnormalities of these syndromes may be a single gene deletion. This review outlines the historical development of the various "22q deletion syndromes," including the DiGeorge, velocardiofacial, Takao, Cayler, and CATCH-22 syndromes, briefly describes the relevant cardiac embryogenesis, and then explains how a single gene deletion may encompass the full phenotypic spectrum.

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Year:  2001        PMID: 11339372     DOI: 10.1097/00125817-200101000-00002

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  2 in total

1.  lncRNA C22orf32-1 contributes to the tumorigenesis of nasopharyngeal carcinoma.

Authors:  Guo-Hui Nie; Zhao Li; Hong-Fang Duan; Liang Luo; Hong-Yi Hu; Wei-Qiang Yang; Li-Ping Nie; Ru-Fei Zhu; Xiao-Fan Chen; Wei Zhang
Journal:  Oncol Lett       Date:  2017-04-11       Impact factor: 2.967

2.  Early-onset psychosis in an adolescent with DiGeorge syndrome: A case report.

Authors:  Keneilwe Molebatsi; Anthony A Olashore
Journal:  S Afr J Psychiatr       Date:  2018-02-21       Impact factor: 1.550

  2 in total

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