Síndrome de deleção 22q11 e cardiopatias congênitas complexas 22q11.2 deletion syndrome and complex congenital heart defects

Síndrome de deleção 22q11 e cardiopatias congênitas complexas 22q11.2 deletion syndrome and complex congenital heart defects

OBJETIVO: Verificar a frequência da síndrome de deleção 22q11 (SD22q11) entre pacientes portadores de cardiopatia congênita do tipo complexa. MÉTODOS: A amostra foi constituída por uma coorte prospectiva e consecutiva de pacientes com cardiopatia complexa em sua primeira hospitalização em uma unidad...

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Bibliographic Details
Main Authors:	Rafael Fabiano Machado Rosa, Patrícia Trevisan, Dayane Bohn Koshiyama, Carlo Benatti Pilla, Paulo Ricardo Gazzola Zen, Marileila Varella-Garcia, Giorgio Adriano Paskulin
Format:	Article
Language:	English
Published:	Associação Médica Brasileira 2011-02-01
Series:	Revista da Associação Médica Brasileira
Subjects:	Síndrome de DiGeorge hibridização in situ fluorescente cardiopatias congênitas cromossomos humanos par 22 DiGeorge syndrome in situ hybridization fluorescence heart defects congenital chromosomes, human, pair 22
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302011000100018

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