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

• প্রধান লেখক: Chih-Ping Chen (লেখক), Chen-Yu Chen (লেখক), Schu-Rern Chern (লেখক), Peih-Shan Wu (লেখক), Shin-Wen Chen (লেখক), Fang-Tzu Wu (লেখক), Wayseen Wang (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Elsevier, 2021-01-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: 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...