Results 11 to 20 of about 8,597 (234)
Small bowel haemorrhage associated with partial midgut malrotation in a middle-aged man [PDF]
We describe a case of life-threatening small bowel haemorrhage in a 56 year old man, who was found to have partial midgut malrotation at laparotomy. An association between congenital malrotation and gastrointestinal haemorrhage has not previously been ...
Peddu Praveen +3 more
doaj +2 more sources
Intestinal malrotation: case description and publication analysis
Intestinal malrotation is a rare congenital anatomical anomaly that results from an abnormal bowel rotation at 10–12 weeks of embryonic development. Clinical manifestations depend on age.
M. V. Simonov +3 more
doaj +1 more source
Background Intestinal malrotation is a rare congenital condition with potentially devastating consequences due to potential volvulus and massive intestinal necrosis.
Sydney A. Martinez +7 more
doaj +1 more source
The growth pattern of the human intestine and its mesentery [PDF]
Supplemental Figures. 3D PDF CS14, CS16, CS20, CS23, and 9.0 and 9.5 WKS. Interactive 3D PDFs are provided for CS14, CS16, CS20, CS23, and 9.0 and 9.5 WKS.
Hayelom K. Mekonen +4 more
core +14 more sources
CONGENITAL INTESTINAL MALROTATION IN ADULT PATIENTS [PDF]
Congenital intestinal malrotation is an impaired embryological development of the gut causing incomplete rotation and attachment of the intestines to the abdominal wall.
Firas Jabir +3 more
doaj +1 more source
A 74-year-old male underwent laparoscopic radical cystectomy for invasive bladder cancer with open surgery for lymph node dissection and urinary diversion (ileal conduit).
Fumito Yamabe +5 more
doaj +1 more source
Acute jaundice as a manifestation of midgut volvulus in a 6-year-old child: A case report
Introduction: Midgut malrotation is a congenital anomaly characterized by the incomplete rotation of the midgut during embryonic development. Although often asymptomatic, midgut malrotation can lead to complications such as midgut volvulus.
Ali Alakbar Nahle +6 more
doaj +1 more source
Novel abdomino-pelvic anomalies in Kagami-Ogata syndrome
Kagami-Ogata syndrome (KOS) is a rare genomic imprinting disorder of chromosome 14 with characteristic facial features, a small, bell-shaped thorax, muscular hypotonia, and abdominal wall defects.
Kelly Lamiman +8 more
doaj +1 more source

