Congenital Heart Disease Revealing Familial 22q11 Deletion Syndrome

Autor: Santos,Marlene Viviane Pires Fernandes, Gamba,Bruno Faulin, Empke,Stefany Lucas Lopes, Alves,Camila Cristina de Oliveira, Bérgamo,Nádia Aparecida, Ribeiro-Bicudo,Lucilene Arilho

Publikováno v: International Journal of Cardiovascular Sciences, Volume: 33, Issue: 4, Pages: 425-426, Published: 03 FEB 2020
International Journal of Cardiovascular Sciences v.33 n.4 2020
International Journal of Cardiovascular Sciences
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC

Congenital heart defects are the most common birth defects and the leading cause of mortality in the first year of life. It is well known that the 22q11 deletion syndrome (22q11DS) is the most common microdeletion syndrome in humans and that congenia

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