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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: 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
التنسيق: Artigo
اللغة:Inglês
منشور في: 1991
الموضوعات:
Research Article
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC1024729/
https://ncbi.nlm.nih.gov/pubmed/1747284
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