Polyhydramnios and abnormal foetal heart rate patterns in a foetus with Prader-Willi syndrome: A case report

Polyhydramnios and abnormal foetal heart rate patterns in a foetus with Prader-Willi syndrome: A case report

Introduction: Prader-Willi syndrome (PWS) is a complex neurodevelopmental genetic disorder. No definitive clinical signs of antenatal PWS have been identified. Case: A healthy, nulliparous, 29-year-old woman demonstrated polyhydramnios at 27 weeks of gestation. Cardiotocography (CTG) showed an absen...

Full description

Bibliographic Details
Main Authors: Tsuyoshi Murata, Toma Fukuda, Aya Kanno, Hyo Kyozuka, Akiko Yamaguchi, Hiromi Shimizu, Takafumi Watanabe, Keiya Fujimori
Format: Article
Language:English
Published: Elsevier 2020-07-01
Series:Case Reports in Women's Health
Subjects:
Prader-Willi syndrome
Polyhydramnios
Abnormal foetal heart rate patterns
Molecular genetic testing
Online Access:http://www.sciencedirect.com/science/article/pii/S2214911220300576

Internet

http://www.sciencedirect.com/science/article/pii/S2214911220300576

Similar Items