Kagami–Ogata syndrome in a fetus presenting with polyhydramnios, malformations, and preterm delivery: a case report

BACKGROUND: Kagami–Ogata syndrome is also known as paternal uniparental disomy 14 and related disorders and is caused by abnormal genomic imprinting in the long arm of the chromosome 14q32.2 region. Its clinical manifestations include polyhydramnios in the fetal stage, respiratory insufficiency beca...

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Detalles Bibliográficos
Autores principales: Huang, Haipeng, Mikami, Yukiko, Shigematsu, Kosuke, Uemura, Nozomi, Shinsaka, Mamiko, Iwatani, Ayaka, Miyake, Fumihito, Kabe, Kazuhiko, Takai, Yasushi, Saitoh, Masahiro, Baba, Kazunori, Seki, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873543/
https://www.ncbi.nlm.nih.gov/pubmed/31753000
http://dx.doi.org/10.1186/s13256-019-2298-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873543/
https://www.ncbi.nlm.nih.gov/pubmed/31753000
http://dx.doi.org/10.1186/s13256-019-2298-y

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