Megacystis Microcolon Intestinal Hypoperistalsis Syndrome: MMIHS View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2019-05-17

AUTHORS

Hideki Soh

ABSTRACT

Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital condition, and such patients tend to present with abdominal distension, a largely dilated nonobstructive bladder, microcolon, and severe functional intestinal obstruction without structural atresia or stenosis in the neonatal period. Currently, the etiology is not well understood, and there is no specific treatment for this condition. The majority of MMIHS patients repeat the intestinal obstruction and enteritis, so they require long-term PN and drainage stomas. The prognosis remains poor. More... »

PAGES

255-259

Book

TITLE

Hirschsprung’s Disease and the Allied Disorders

ISBN

978-981-13-3605-8
978-981-13-3606-5

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-981-13-3606-5_40

DOI

http://dx.doi.org/10.1007/978-981-13-3606-5_40

DIMENSIONS

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