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

Internet

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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