Literature DB >> 11015695

Megacystis-microcolon-intestinal hypoperistalsis syndrome: the difficulties with antenatal diagnosis. Case report and review of the literature.

S M White1, P Chamberlain, R Hitchcock, P B Sullivan, P A Boyd.   

Abstract

Megacystis on antenatal scan in female fetuses is rare and has serious diagnostic implications. We report two cases of megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) in female infants in whom antenatal scan abnormalities were identified, but the diagnosis not made until after delivery. MMIHS is a rare autosomal recessive condition which is usually lethal in the first year of life. Prenatal diagnosis is hampered by the lack of specific diagnostic findings on ultrasound and the absence of an identified genetic locus. The prenatal findings in MMIHS are reviewed and contrasted with those of other causes of lower abdominal masses on antenatal ultrasound. Copyright 2000 John Wiley & Sons, Ltd.

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Year:  2000        PMID: 11015695     DOI: 10.1002/1097-0223(200009)20:9<697::aid-pd891>3.0.co;2-o

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

Review 1.  Familial megacystis microcolon intestinal hypoperistalsis syndrome: a systematic review.

Authors:  Danielle Mc Laughlin; Prem Puri
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

2.  An unusual urinary tract presentation in a case of megacystis microcolon intestinal hypoperistalsis syndrome.

Authors:  Melkamu Adeb; Sudha Anupindi; Michael Carr; Kassa Darge
Journal:  J Radiol Case Rep       Date:  2012-11-01
  2 in total

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