Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother

• Auteurs principaux: Chih-Ping Chen (Auteur), Chen-Yu Chen (Auteur), Schu-Rern Chern (Auteur), Peih-Shan Wu (Auteur), Shin-Wen Chen (Auteur), Fang-Tzu Wu (Auteur), Wayseen Wang (Auteur)
• Format: Livre
• Publié: Elsevier, 2021-01-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Objective: We present prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother. Case report: A 28-year-old woman primigravid underwent amniocentesis at 23 weeks of gestation because of fetal ultrasoun...