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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...

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Main Authors:	Tsuyoshi Murata (Author), Toma Fukuda (Author), Aya Kanno (Author), Hyo Kyozuka (Author), Akiko Yamaguchi (Author), Hiromi Shimizu (Author), Takafumi Watanabe (Author), Keiya Fujimori (Author)
Format:	Book
Published:	Elsevier, 2020-07-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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