Results 41 to 50 of about 2,226 (184)
A case report of a 30-year-old male with megacystis-microcolon-intestinal hypoperistalsis syndrome with de novo ACTG2 gene mutation [PDF]
Hospital Pharmacology, 2023 Introduction: Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a very rare genetic disorder of visceral motility of the gastrointestinal and genitourinary system.
Knežević Violeta V. +4 more
doaj +1 more source
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.
core +1 more source
EP06.38: Pop‐off mechanisms in fetal megacystis: extravasation, umbilical cord cyst, ureterocele and mega‐ureter [PDF]
Ultrasound in Obstetrics & GynecologyUCC was associated with early-onset megacystis, normal AFI, other congenital anomalies and the highest prevalences of IUFD, while the occurrence of urinary extravasation was associated with an antenatal clinical picture characterised by severe megacystis,
L. Brinkman +9 more
semanticscholar +2 more sources
Changes in cardiac morphometry in fetuses with lower urinary tract obstruction. [PDF]
Pregnancy (Hoboken)Abstract Objective Fetal lower urinary tract obstruction (LUTO) is associated with significant perinatal morbidity due to oligohydramnios, pulmonary hypoplasia, and progressive renal dysfunction. In addition to these well‐known sequelae, LUTO has been linked to various cardiac abnormalities on prenatal imaging, including cardiomegaly; ventricular ...
Araji S +10 more
europepmc +2 more sources
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
doaj +1 more source
Diagnostics, 2023 This article presents a rare case of cloacal dysgenesis sequence (CDS) detected at 23 weeks of gestation in a 36-year-old woman’s first ongoing pregnancy.
Nicolae Gică +5 more
doaj +1 more source
Archives of Gynecology and Obstetrics, 2023 Objectives To assess the spectrum of underlying pathologies, the intrauterine course and postnatal outcome of 46 fetuses with megacystis that underwent intrauterine vesico-amniotic shunting (VAS) with the Somatex® shunt in a single center.
I. Gottschalk +12 more
semanticscholar +1 more source
Isolated congenital megacystis without intestinal obstruction: A mild variant of chronic intestinal pseudoobstruction syndrome? [PDF]
, 2011 Megacystis is frequently involved with chronic intestinal pseudoobstruction syndrome; however, isolated megacystis without intestinal obstruction is extremely rare.
47 +26 more
core +1 more source
Megacystis secondary to myenteric plexus pathology - Presentation of two cases
, 2021 Herein, 2 cases of megacystis secondary to myenteric plexus pathology are reported. Unlike the entity of visceral myopathy, there was ganglion cell loss both in the bladder and in the colon of these 2 cases.
Serel, TA +5 more
core +1 more source
Recurrent UTIs in Children With CAKUT
Journal of Paediatrics and Child Health, EarlyView.ABSTRACT Congenital abnormalities of the kidney and urinary tract (CAKUT) encompass diverse diagnoses that commonly present as urinary tract dilatation and are the leading cause of kidney failure in children. Antenatal hydronephrosis occurs in ~1% of pregnancies; most resolve spontaneously, but conditions such as posterior urethral valves (PUV ...
Lucielle Standish +6 more
wiley +1 more source