22q11 Deletion Syndrome with Vascular Anomalies
22q11 Deletion Syndrome with Vascular Anomalies
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Author / Creator
Publisher
United States: Wolters Kluwer India Pvt. Ltd
Journal title
Language
English
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Publication information
Publisher
United States: Wolters Kluwer India Pvt. Ltd
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Scope and Contents
Contents
DiGeorge syndrome, also termed 22q11.2 deletion syndrome, represents a spectrum of disorders that include thymic aplasia/hypoplasia, parathyroid aplasia/hypoplasia, conotruncal vascular anomalies, and velocardiofacial (Shprintzen) syndrome. This case report describes a novel constellation of cardiovascular anomalies in a 31-year-old patient with 22...
Alternative Titles
Full title
22q11 Deletion Syndrome with Vascular Anomalies
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5801571
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5801571
Other Identifiers
ISSN
2156-7514
E-ISSN
2156-5597,2156-7514
DOI
10.4103/jcis.JCIS_66_17
