罕见病知识库 RareSeen

先天性致死性红皮病

Congenital lethal erythroderma

ORPHA:1954疾病

定义 英文原文(暂无中文)

A rare skin disorder characterized by erythrodermic, peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhea, failure to thrive and severe hypoalbuminaemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992.

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 9

极常见 99–80%9

  • 先天性剥脱性红皮病 HP:0007381
  • 婴儿期夭折 HP:0001522
  • 干性皮肤 HP:0000958
  • 发育迟滞 HP:0001508
  • 低蛋白血症 HP:0003073
  • 鱼鳞病 HP:0008064
  • 吸收不良 HP:0002024
  • 呼吸功能不全 HP:0002093
  • 荨麻疹 HP:0001025

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)