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

被引：0

作者：

Haipeng Huang

Yukiko Mikami

Kosuke Shigematsu

Nozomi Uemura

Mamiko Shinsaka

Ayaka Iwatani

Fumihito Miyake

Kazuhiko Kabe

Yasushi Takai

Masahiro Saitoh

Kazunori Baba

Hiroyuki Seki

机构：

[1] Saitama Medical Center,Department of Obstetrics and Gynecology

[2] Saitama Medical University,Department of Pediatrics, Saitama Medical Center

[3] Saitama Medical University,undefined

来源：

Journal of Medical Case Reports | / 13卷

关键词：

Kagami–Ogata syndrome; Genetic diagnosis; Epigenetic mutation; Amniodrainage; Fetal diagnosis;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

共 25 条

[1]

Li E(1993)Role for DNA methylation in genomic imprinting Nature 366 362-365

[2]

Beard C(2008)Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd (14)-like phenotypes Nat Genet 40 237-242

[3]

Jaenisch R(2012)Paternal uniparental disomy 14 and related disorders: placental gene expression analyses and histological examinations Epigenetics 7 1142-1150

[4]

Kagami M(2015)Comprehensive clinical studies in 34 patients with molecularly defined UPD (14) pat and related conditions (Kagami-Ogata syndrome) Eur J Hum Genet 23 1488-1498

[5]

Sekita Y(2011)Radiological evaluation of dysmorphic thorax of paternal uniparental disomy 14 Pediatr Radiol 41 1013-1019

[6]

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[7]

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[8]

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[9]

Okada M(undefined)undefined undefined undefined undefined-undefined

[10]

Kagami M(undefined)undefined undefined undefined undefined-undefined

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