多指(趾)并指(趾)畸形-心脏畸形综合征
Polysyndactyly-cardiac malformation syndrome
定义 英文原文(暂无中文)
A rare, life-threatening developmental defect during embryogenesis characterized by polysyndactyly of fingers and toes as well as complex congenital heart defects (e.g. atrioventricular septal defects, aortic dextroposition, single ventricle, hypo- or hypertrophy of one side of the heart). Additional features may include dysmorphic traits (large fontanel, high forehead, ptosis, hypertelorism, epicanthus, low-set malformed ears, prominent root of the nose, bulbous nose, anteverted nares, long and smooth philtrum, thin upper lip, micrognathism, hirsutism, single transverse crease) nail hypoplasia, phalange agenesis/hypoplasia, flexion contractures, polysplenia, multiple hepatic/renal cysts, atrophic biliary vesicle, ductal plate malformation and genital anomalies (e.g. micropenis, undescended testes, hypoplastic scrotum). The syndrome is usually fatal in utero or in infancy, but survival cases have been reported.
别名
Bonneau综合征
基本事实
- 遗传方式
- 常染色体隐性
- 发病年龄
- 婴儿期、新生儿期
- 患病率
- <1 / 1 000 000
临床表型 18
极常见 99–80%3
- 心脏形态异常 HP:0001627
- 多指(趾)畸形 HP:0010442
- 并指(趾)畸形 HP:0001159
常见 79–30%9
- 鼻孔前翻 HP:0000463
- 房间隔缺损 HP:0001631
- 蒜头鼻 HP:0000414
- 眼距过宽 HP:0000316
- 低位耳 HP:0000369
- 肝管板畸形 HP:0006563
- 小下颌 HP:0000347
- 羊水过多 HP:0001561
- 室间隔缺损 HP:0001629
偶见 29–5%6
- 白内障 HP:0000518
- 内眦赘皮 HP:0000286
- 小眼症 HP:0000568
- 肾皮质囊肿 HP:0000803
- 法洛四联症 HP:0001636
- 玻璃体出血 HP:0007902
外部标识与链接
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本页数据来源
- 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
- 中文病名:Orphanet 中文包,冻结于 2020-06-01
- 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)