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DiGeorge Syndrome is a medical term for a set of symptoms which are part of what is now understood to be 22q11.2 deletion syndrome. Angelo DiGeorge, for whom the syndrome is named, described four children in 1965 with the triad of thymic hypoplasia, hypoparathyroidism, and recurrent infection. As further cases were investigated, the syndrome came to be known as DiGeorge association, and to encompass congenital cardiac anomalies, craniofacial malformations, and learning dysfunction due to defects in the third and fourth pharyngeal pouches during embryogenesis.

Genetic disorders | Eponymous diseases

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22q and You Center - Symptoms, diagnosis, and treatment of chromosome 22q11.2 deletion, a genetic disorder associated with DiGeorge, velocardiofacial and other syndromes.
Meta Description: [ Providing diagnosis, treatment and management of children with chromosome 22q11.2 deletion. Learn more about DiGeorge, velocardiofacial and other syndromes caused by this genetic disorder. ]

National Library of Medicine: DGS - DiGeorge syndrome, the synonyms, a summary and list of major features.

Yahoo! Clubs VCFS Family Support - Join, post and read mail for this group which concerns DiGeorge Syndrome and Velo-Cardio-Facial Syndrome.
Meta Description: [ vcfsfamilysupport: A Place To Chat About Our Kids! ]

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