Results 31 to 40 of about 1,107 (148)
Radiology Case Reports, 2021 Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital defect of the bowel and bladder that is especially rare in males.
Jennifer Lim, BS +2 more
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Megacystis microcolon intestinal hypoperistalsis syndrome: a report of a variant [PDF]
, 2018 Megacystis microcolon intestinal hypoperistalsis syndrome is a very rare cause of functional intestinal obstruction in newborns. It is associated with nonobstructed distended urinary bladder, microcolon, and decreased or absent intestinal peristalsis ...
Al-Salem, Ahmed H.
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Megacystis-Microcolon–Intestinal Hypoperistalsis Syndrome: A Case Report [PDF]
, 2022 A 1-day-old girl, late preterm (36 weeks 3 days) infant, was admitted to the neonatal intensive care unit for respiratory distress and megacystis seen on a prenatal ultrasound at 24 weeks of gestation. A babygram (anteroposterior view of the entire body)
Chen, Johnathan, Kinzel, Adam James
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Ultrasound prenatal diagnosis of typical megacystis, microcolon, intestinal hypoperistalsis syndrome
Clinical Case Reports, 2018 Key Clinical Message In the presence of megacystis in the second half of pregnancy, with increased amniotic fluid, especially in a female fetus, the most likely diagnostic result is megacystis, microcolon, intestinal hypoperistalsis syndrome, MMIHS.
Natalia Buinoiu +5 more
doaj +1 more source
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome [PDF]
, 2007 We report a case of megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) in a newborn female infant who presented with an abdominal mass, absent bowel sounds, and feeding intolerance with bilious emesis.
Clark, Paul, O'Connor, Stephen C.
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Congenital absence of jejunum and ileum: A case report and literature review
African Journal of Paediatric Surgery, 2017 We report an extremely rare finding 'congenital absence of jejunum and ileum' during explorative laparotomy of a 16-day-old female neonate. The dilated duodenum was terminating blindly, and the next segment of intestine was a peanut-sized cecum followed ...
Prasanta Kumar Tripathy +2 more
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Congenital multiple colonic atresias with intestinal malrotation: a case report
Surgical Case Reports, 2020 Background Congenital intestinal atresia develops in 1 in 1500 to 20,000 births. Colonic atresia, which accounts for 1.8–15% of intestinal atresia cases, is accompanied by other gastrointestinal atresias such as small intestinal atresia, gastroschisis ...
Daisuke Ishii +3 more
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Ileal atresia with intraluminal Meckel's diverticulum
Journal of Pediatric Surgery Case Reports, 2023 Background: Jejuno-ileal atresia is a major cause of neonatal intestinal obstruction with a prevalence of 1.8 per 10 000 live births. It is thought to arise from intrauterine vascular accident.
Ibrahim Ali Ibrahim +1 more
doaj +1 more source
, 1995 HYDROMETROCOLPOS AND SEGMENTAL COLONIC DILATATION IN A GIRL WITH MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS ...
David Watters (13099569) +6 more
core +2 more sources
Case Reports in Gastrointestinal Medicine, 2021 MMIHS, also known as Berdon’s syndrome, is a rare disease that belongs to primary causes of CIPOS (chronic intestinal pseudoobstruction syndrome). Clinical characteristics of MMIHS are differential, but we come across the following classic symptoms ...
Katarzyna Ignasiak-Budzyńska +2 more
doaj +1 more source