并腿畸形
Sirenomelia
定义 英文原文(暂无中文)
A rare, lethal, congenital anomaly that may represent the most severe form of caudal dysgenesia and characterized by fusion of the lower limbs (mermaid-like) always associated with severe genitourinary and gastrointestinal anomalies. Furthermore, there is wide phenotipical variability in the musculoskeletal, central nervous system, cardiopulmonary, anomalies present. Pelvic, sacral and spinal defects , internal and external genitalia defects, renal agenesis, absent bladder, rectal/anal atresia are commonly described. Most cases are stillborn or die during, or shortly after, birth. Sirenomelia can be classified on the basis of limb malformations phenotypes. Due to the similarity, the distinction between sirenomelia and caudal regression syndrome, familial caudal dysgenesis and VACTERL is debated.
基本事实
- 遗传方式
- 不适用
- 发病年龄
- 产前、新生儿期
- 患病率
- 1-9 / 100 000(France)
临床表型 10
极常见 99–80%6
- 泌尿系统异常 HP:0000079
- 骶骨缺如 HP:0010305
- 外阴性别不明 HP:0000062
- 肛门闭锁 HP:0002023
- 肾发育不良/不全 HP:0008678
- 美人鱼综合症(并腿畸形) HP:0010497
常见 79–30%4
- 心血管系统的任何异常。 HP:0001626
- 桡骨发育不良/发育不全 HP:0006501
- 脊柱裂 HP:0002414
- 气管食管瘘 HP:0002575
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)