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家族性肠道旋转不良

Familial intestinal malrotation

ORPHA:508410疾病

定义 英文原文(暂无中文)

A rare familial intestinal malformation characterized by failure of the rotation of the developing gastrointestinal tract around the superior mesenteric artery during embryonic development, resulting in a spectrum of abnormalities of intestinal position and fixation. Patients most typically present in the neonatal period with midgut volvulus, which can lead to short bowel syndrome or even death. Signs and symptoms include bilious vomiting, feeding intolerance, failure to thrive, constipation, bloody stools, or intermittent apnea. The condition may also manifest later in life with complications like kinking or hernias and a broad range of intestinal symptoms. It can be an isolated finding or occur in association with other anomalies.

基本事实

发病年龄
各年龄段

临床表型 8

极常见 99–80%8

  • 鼻孔前翻 HP:0000463
  • 鼻梁塌陷 HP:0005280
  • 前额突出 HP:0002007
  • 额头高 HP:0000348
  • 眼距过宽 HP:0000316
  • 肠旋转不良 HP:0002566
  • 睑裂增宽 HP:0000637
  • 肠扭转 HP:0002580

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)