König P, Ambrose N S, Scott N
Department of Colorectal Surgery of St James's University Hospital, Leeds, UK.
Eur J Gastroenterol Hepatol. 2000 Jan;12(1):127-8. doi: 10.1097/00042737-200012010-00023.
Hereditary internal anal sphincter myopathy is a very rare condition, only three families have so far been described in the literature. In this case report further clinical and histological findings of one affected member of one of the above families are presented.
遗传性肛门内括约肌肌病是一种非常罕见的疾病,迄今为止文献中仅描述了三个家族。在本病例报告中,呈现了上述家族中一名患病成员的进一步临床和组织学发现。