Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.

M. Y. Chung; C. B. Huang; J. H. Chuang; S. F. Ko; L. Chen

Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.

M. Y. Chung^*, C. B. Huang, J. H. Chuang, S. F. Ko, L. Chen

^*此作品的通信作者

Chang Gung Memorial Hospital

研究成果: 期刊稿件 › 文章 › 同行評審

7 引文斯高帕斯（Scopus）

摘要

Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disorder characterized by a massively enlarged urinary bladder without mechanical outlet obstruction and microcolon, as well as a hypoperistaltic bowel with normal ganglion cell distribution. We report one such case to discuss the findings of antenatal ultrasound and the radiologic and pathologic features of this condition.

原文	英語
頁（從 - 到）	92-96
頁數	5
期刊	Chang Gung Medical Journal
卷	21
發行號	1
出版狀態	已出版 - 03 1998
對外發佈	是

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title = "Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.",

abstract = "Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disorder characterized by a massively enlarged urinary bladder without mechanical outlet obstruction and microcolon, as well as a hypoperistaltic bowel with normal ganglion cell distribution. We report one such case to discuss the findings of antenatal ultrasound and the radiologic and pathologic features of this condition.",

author = "Chung, {M. Y.} and Huang, {C. B.} and Chuang, {J. H.} and Ko, {S. F.} and L. Chen",

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AU - Huang, C. B.

AU - Chuang, J. H.

AU - Ko, S. F.

AU - Chen, L.

PY - 1998/3

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N2 - Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disorder characterized by a massively enlarged urinary bladder without mechanical outlet obstruction and microcolon, as well as a hypoperistaltic bowel with normal ganglion cell distribution. We report one such case to discuss the findings of antenatal ultrasound and the radiologic and pathologic features of this condition.

AB - Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disorder characterized by a massively enlarged urinary bladder without mechanical outlet obstruction and microcolon, as well as a hypoperistaltic bowel with normal ganglion cell distribution. We report one such case to discuss the findings of antenatal ultrasound and the radiologic and pathologic features of this condition.

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M3 - 文章

C2 - 9607272

AN - SCOPUS:0032018905

SN - 0255-8270

VL - 21

SP - 92

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JO - Chang Gung Medical Journal

JF - Chang Gung Medical Journal

IS - 1

ER -

Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): a case report.

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