Clinical course and genetic analysis of a case of the amniocentesis showing chromosome 6 trisomy mosaicism

• Egile Nagusiak: Naoya Kitamura (Egilea), Yuki Ito (Egilea), Tomoko Kawai (Egilea), Hiromi Kamura (Egilea), Michihiro Yamamura (Egilea), Haruna Okubo (Egilea), Akihiro Hasegawa (Egilea), Momoko Inoue (Egilea), Ken Takahashi (Egilea), Michiko Miya (Egilea), Hiroshi Kawame (Egilea), Osamu Samura (Egilea), Aikou Okamoto (Egilea)
• Formatua: Liburua
• Argitaratua: Elsevier, 2024-05-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Objective: Herein, we present a case of mosaic trisomy 6 detected by amniocentesis. Case report: Amniocentesis (G-banding) was performed at 17 weeks of gestation; the results were 47,XY,+6[3]/46,XY[12]. Fetal screening ultrasonography showed no morphological abnormalities, and the parents desired to...