AXONAL DYSTROPHY PRESENTING AS THE MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME

被引：18

作者：

ALRAYESS, M

AMBLER, MW

机构：

[1] RHODE ISL HOSP,DEPT PATHOL,NEUROPATHOL SECT,593 EDDY ST,PROVIDENCE,RI 02903

[2] YALE UNIV,SCH MED,NEUROPATHOL SECT,NEW HAVEN,CT 06510

来源：

PEDIATRIC PATHOLOGY | 1992年 / 12卷 / 05期

关键词：

MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME; AXONAL DYSTROPHY;

D O I：

10.3109/15513819209024229

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a neonatal intestinal syndrome, characterized by defective peristalsis and bladder dilatation, refractory to pharmacological treatment. Examinations of bowel and bladder have failed to demonstrate a pathological explanation for this syndrome. We describe a 7-month-old female infant with MMIHS who had generalized axonal dystrophy of her central, peripheral, and autonomic nervous systems, which may provide a neuropathological explanation for some cases of MMIHS.

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页码：743 / 750

页数：8

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