A Novel Mutation in ACTG2 Gene in Mother with Chronic Intestinal Pseudoobstruction and Fetus with Megacystis Microcolon Intestinal Hypoperistalsis Syndrome [PDF]
Case Reports in Genetics, 2017 Background. A novel mutation in the ACTG2 gene is described in a pregnant patient followed up for chronic intestinal pseudoobstruction (CIPO) during pregnancy and her fetus with megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS). Case.
Julie R. Whittington +3 more
doaj +2 more sources
Fetal Magnetic Resonance Imaging of Megacystis microcolon intestinal hypoperistalsis syndrome
Jurnal Prima Medika SainsMegacystis microcolon intestinal hypoperistalsis syndrome (MMIHs) is a rare congenital anomaly, involve urinary tract and gastrointestinal tract. The prognosis is dismal, the death is caused by infection.
D. A. Wirasasmita, Alexandra Sachlan
semanticscholar +2 more sources
Case Reports in Perinatal MedicineTo describe the prenatal diagnosis, unique clinical features, clinical and genetic evaluation, and the pregnancy and neonatal course of two siblings affected by Lethal Congenital Contractural Syndrome 2 (LCCS2).
Hatjis Christos G. +4 more
doaj +2 more sources
Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): challenges in diagnosis and management. [PDF]
BMJ Case RepMegacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare, congenital functional intestinal obstruction, characterised by megacystis (bladder distention in the absence of mechanical obstruction), microcolon and intestinal ...
Murali K, Dhua AK.
europepmc +2 more sources
Antenatal Determinants of Postnatal Renal Function in Fetal Megacystis: A Systematic Review
DiagnosticsIntroduction: To evaluate the clinical usefulness of demographic data, fetal imaging findings and urinary analytes were used for predicting poor postnatal renal function in children with congenital megacystis.
Ugo Maria Pierucci +6 more
doaj +2 more sources
Do certain drugs cause the megacystis-microcolon-intestinal hypoperistalsis syndrome
The Turkish Journal of Pediatrics, 1989 A case of megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) in the offspring of a mother who had ingested scopolamine, trimethoprim-sulfadiazine and dipyrone during pregnancy is presented.
H Doğruyol
doaj +3 more sources
Fetoscopic Vesicostomy for Lower Urinary Tract Obstruction: A Proposal for a New Surgical Technique. [PDF]
Prenat DiagnPrenatal Diagnosis, Volume 46, Issue 9, Page 1468-1471, August 2026.
Miranda ML +5 more
europepmc +2 more sources
Megacystis microcolon intestinal hypoperistalsis syndrome complicated by perforation.
African Journal of Paediatric SurgeryMegacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a quite rare congenital and fatal disease. The disease is three to four times more prevalent in females than males. Most of the cases die within the early months of their lives.
V. Jain +3 more
semanticscholar +2 more sources
Megacystis microcolon intestinal hypoperistalsis syndrome complicated by perforation
African Journal of Paediatric Surgery, 2011 Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a quite rare congenital and fatal disease. The disease is three to four times more prevalent in females than males. Most of the cases die within the early months of their lives.
Jain Vishal +3 more
doaj +2 more sources
De Novo RRAS2 Pathogenic Variant in a Fetus With Bilateral Radial Ray and Multisystem Anomalies. [PDF]
Prenat DiagnPrenatal Diagnosis, Volume 46, Issue 4, Page 603-606, April 2026.
Legro NR +3 more
europepmc +2 more sources