The megacystis microcolon intestinal hypoperistalsis syndrome: report of a case. J Pediatr Surg 1981 Oct;16(5):749-51
Date
10/01/1981Pubmed ID
7031220DOI
10.1016/s0022-3468(81)80571-4Scopus ID
2-s2.0-0019489546 (requires institutional sign-in at Scopus site) 38 CitationsAbstract
An infant girl with the megacystis microcolon intestinal hypoperistalsis syndrome is reported. The presence of polyhydramnios and the absence of upper urinary tract abnormalities, differentiate this patient from similar cases previously reported. Although the etiology of this disease is unknown, partial success with the use of bethanechol suggests that the deranged intestinal motility may be related to dysfunction of the autonomic nerve endings of the gut.
Author List
Jona JZ, Werlin SLAuthor
Steven L. Werlin MD Emeritus Professor in the Pediatrics department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
ColonFemale
Gastrointestinal Motility
Humans
Infant, Newborn
Intestinal Obstruction
Peristalsis
Polyhydramnios
Pregnancy
Syndrome
Urinary Bladder Diseases









