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Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.

We report on a prenatal diagnosis by FISH of a familial 22q11 deletion associated with DiGeorge syndrome (DGS). The deletion was seen in the proband with symptoms of full DGS, in the physically normal father, and in a subsequent pregnancy. After birth this child showed hypocalcaemia, a T cell defici...

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Detalhes bibliográficos
Main Authors: Van Hemel, J O, Schaap, C, Van Opstal, D, Mulder, M P, Niermeijer, M F, Meijers, J H
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051646/
https://ncbi.nlm.nih.gov/pubmed/7473663
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