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
Publicado en:J Med Case Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado: BioMed Central 2019
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6873543/
https://ncbi.nlm.nih.gov/pubmed/31753000
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-019-2298-y
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