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肢端肾综合征

Acrorenal syndrome

ORPHA:971疾病

定义 英文原文(暂无中文)

A spectrum of congenital malformative disorders characterized by the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (e.g. unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract (genital anomalies, ureteral hypoplasias, vesicoureteral reflux), abdominal well defects, intestinal atresias, and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected.

基本事实

遗传方式
常染色体隐性
发病年龄
新生儿期
患病率
<1 / 1 000 000

临床表型 11

极常见 99–80%3

  • 肾形态异常 HP:0012210
  • 肾发育不良/不全 HP:0008678
  • 手劈裂 HP:0001171

常见 79–30%4

  • 尺骨形态异常 HP:0040071
  • 胫骨形态异常 HP:0002992
  • 桡骨发育不良/发育不全 HP:0006501
  • 肾功能不全 HP:0000083

偶见 29–5%4

  • 眼部异常 HP:0000478
  • 视力异常 HP:0000504
  • 腭裂 HP:0000175
  • 小下颌 HP:0000347

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)