| Literature DB >> 11339372 |
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.Entities:
Mesh:
Substances:
Year: 2001 PMID: 11339372 DOI: 10.1097/00125817-200101000-00002
Source DB: PubMed Journal: Genet Med ISSN: 1098-3600 Impact factor: 8.822