Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation

• Váldodahkkit: Xia Li (Dahkki), Lan-Zhen Zhang (Dahkki), Lin Yu (Dahkki), Zhao-Lua Long (Dahkki), An-Yun Lin (Dahkki), Chen-Yu Gou (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: BMC, 2021-05-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Abstract Background Meier-Gorlin syndrome 7 (MGS7) is a rare autosomal recessive condition. We reported a fetus diagnosed with Meier-Gorlin syndrome 7. The antenatal sonographic images were presented, and compound heterozygous mutations of CDC45 on chromosome 22 were identified by whole-exome sequen...