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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Format: | Book |
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Elsevier,
2020-07-01T00:00:00Z.
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A1234.567 |
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