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Familial autonomic visceral myopathy with degeneration of muscularis mucosae.

机译:家族性内脏肌病伴粘膜肌变性。

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摘要

An extended family with chronic intestinal pseudo-obstruction which affected 11 of 54 members was studied. Patients presented with recurrent intestinal obstruction in childhood or adolescence: eight of the 11 died before the age of 30. Pedigree analysis showed four consanguineous marriages. The patients were all in the fifth generation and had established an autosomal recessive mode of inheritance. Histological, immunocytochemical, and electron microscopic studies were performed on a colectomy specimen from a surviving affected family member. Familial visceral myopathy was diagnosed--characterised by degeneration and collagenous replacement of both layers of the muscularis propria and the muscularis mucosae.
机译:研究了一个患有慢性肠道假性阻塞的大家庭,该家庭影响了54名成员中的11名。患者在儿童期或青春期出现肠梗阻复发:11例中有8例在30岁之前死亡。家谱分析显示有4例近亲结婚。这些患者均为第五代患者,并建立了常染色体隐性遗传方式。对幸存的受影响家庭成员的结肠切除术标本进行了组织学,免疫细胞化学和电子显微镜研究。诊断为家族性内脏肌病-其特征是固有肌层和粘膜肌层的变性和胶原蛋白置换。

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