DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.

DiGeorge syndrome was diagnosed in an infant who had an interrupted aortic arch, hypoparathyroidism, and low T lymphocyte numbers. Two siblings had heart defects that are not commonly described in DiGeorge syndrome (a membranous ventricular septal defect and coarctation of the aorta respectively). T...

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Detalhes bibliográficos
Main Authors: Wilson, D I, Cross, I E, Goodship, J A, Coulthard, S, Carey, A H, Scambler, P J, Bain, H H, Hunter, A S, Carter, P E, Burn, J
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1024729/
https://ncbi.nlm.nih.gov/pubmed/1747284
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