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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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Detalles Bibliográficos
Autores principales:	Murata, Tsuyoshi, Fukuda, Toma, Kanno, Aya, Kyozuka, Hyo, Yamaguchi, Akiko, Shimizu, Hiromi, Watanabe, Takafumi, Fujimori, Keiya
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283086/ https://www.ncbi.nlm.nih.gov/pubmed/32528861 http://dx.doi.org/10.1016/j.crwh.2020.e00227

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