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Murine Ileocolic Bowel Resection with Primary Anastomosis
Published on: October 29, 2014
A case report of adult congenital intestinal malrotation
Yu Gao1,2, Xiaobiao Song1, Qiang Song1
1Department of Gastrointestinal Surgery, Baotou Central Hospital, Baotou, China.
Insights
Congenital intestinal malrotation, a rare digestive anomaly, occurs when fetal intestines fail to rotate correctly. This can cause serious complications, necessitating timely diagnosis and treatment in adults.
Area of Science:
- Gastroenterology
- Pediatric Surgery
- Developmental Biology
Background:
- Congenital intestinal malrotation is a rare anomaly from abnormal fetal intestinal rotation and fixation.
- It can lead to life-threatening complications like volvulus, obstruction, and necrosis.
- While common in neonates, it also affects adults, often with delayed diagnosis due to nonspecific symptoms.
Abstract:
Congenital intestinal malrotation is a rare congenital digestive tract anomaly, primarily due to the failure of the intestines to rotate and fix properly within the peritoneal cavity during fetal development. This abnormality can lead to severe complications such as intestinal volvulus, intestinal obstruction, and even intestinal necrosis. Although the condition is more commonly seen in neonates, cases in adults have also been reported, often with delayed diagnosis due to atypical symptoms. In this article, we will discuss the diagnosis and treatment of congenital intestinal malrotation in adults.
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