Results 101 to 110 of about 620,878 (264)

Congenital multiple colonic atresias with intestinal malrotation: a case report

Surgery 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 ...
D. Ishii, H. Miyagi, M. Hirasawa, K. Miyamoto   +3 more
semanticscholar   +1 more source

Case Report: A Rare Gastrojejunal Connection Causing Internal Hernia

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Internal hernias are rare and often difficult to diagnose due to their nonspecific clinical presentation. We describe an unusual case of an internal hernia caused by an abnormal gastrojejunal connection, incidentally identified during a laparoscopic appendectomy.
Jingjun Yang, Chenfei Jiang
wiley   +1 more source

Utility of the CT Scan in Diagnosing Midgut Volvulus in Patients with Chronic Abdominal Pain

Case Reports in Surgery, 2017
Symptomatic intestinal malrotation first presenting in the adults is rare. Midgut volvulus is the most common complication of malrotation in the adults.
Ehsan Shahverdi, Mehdi Morshedi, Maryam Allahverdi Khani, Mohammad Baradaran Jamili, Fatemeh Shafizadeh Barmi   +4 more
doaj   +1 more source

Prenatal MRI Detection of Fetal Small Intestinal Volvulus: The Black‐and‐White and Coffee‐Bean Signs

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT A rare case of fetal small intestinal volvulus was diagnosed prenatally using MRI, with characteristic black‐and‐white and coffee‐bean signs. Early diagnosis led to timely surgical intervention and a favorable outcome.
Miyu Nakamura, Hiroshi Sato, Kazuyo Kakui   +2 more
wiley   +1 more source

Primary cilia are specialized calcium signaling organelles [PDF]

, 2014
Summary Primary cilia are solitary nonmotile extensions of the centriole found on nearly all nucleated eukaryotic cells between cell divisions. Only ∼200-300 nm in diameter and a few microns long, they are separated from the cytoplasm by the ciliary neck
Clapham, David E., DeCaen, Paul G., Delling, Markus, Doerner, Julia F., Febvay, Sebastien   +4 more
core   +1 more source

Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations [PDF]

, 2018
Smooth muscle dysfunction syndrome (SMDS) due to heterozygous ACTA2 arginine 179 alterations is characterized by patent ductus arteriosus, vasculopathy (aneurysm and occlusive lesions), pulmonary arterial hypertension, and other complications in smooth ...
A Kikuchi, Alan C Braverman, AN Moosa, Anji Yetman, Anna L Mitchell, Anne Child, Anthony Estrera, AT Yetman, Birgit Lorenz, BL Loeys, Cori Feist, Denver Sallee, Dianna M Milewicz, DJ Schneider, DM Milewicz, Ellen S Regalado, ES Regalado, ES Roach, FM Roulez, Glen Iannucci, Hiroko Morisaki, HU Moller, J de Grazia, J Richer, JL Anderson, John R Ostergaard, Julie De Backer, Julie Richer, Kathryn C Chatfield, Kathryn W Holmes, Lauren Mellor-Crummey, LC Ades, Lesley Ades, LW Fung, M Al-Mohaissen, M Elizabeth Brickner, M Keir, MC Brodsky, ME Meuwissen, MM Georgescu, MR Amans, Mustafa Tekin, NJ Ullrich, P Munot, Patricia Musolino, Paul Mark, Reed Pyeritz, RV Lacro, S Prabhu, Shaine A Morris, Sherene Shalhub, Susan Benedict, T Logeswaran, Takayuki Morisaki, Timothy J Bradley, Y Arlachov   +55 more
core   +3 more sources

Pelvi‐Ureteric Junction Obstruction in a Solitary Functioning Kidney in Children: An Unfavourable Combination

Acta Paediatrica, Volume 115, Issue 1, Page 196-201, January 2026.
ABSTRACT Aim Solitary functioning kidney (SFK) is linked to chronic kidney disease (CKD) in children, particularly when associated with congenital anomalies of the kidney and urinary tract (CAKUT). Pelvi‐ureteric junction obstruction (PUJO) is the most frequent obstructive uropathy in SFK.
Mathilde Grapin, Lucas Rabaux, Mathilde Glenisson, Eva Mille, Nathalie Biebuyck, Evgenia Preka, Olivia Boyer, Kiarash Taghavi, Guillaume Dorval, Thomas Blanc   +9 more
wiley   +1 more source

Malrotation of intestine with Carcinoma Colon in adult AUTHORS Dr. Dipankar Ray MS DNB FRCS* Prof. Gautam Chattopadhyay MS FRCS Dr. Surajit Das MS * Assistant Professor, Department of Surgical Gastroenterology Medical College Kolkata

Journal of Nepal Medical Association, 2014
Malrotation of gut is a congenital anomaly and patients usually present in childhood. Occasionally it may present in adulthood. Patients are usually asymptomatic when malrotation of gut is detected during investigations, operation or autopsy. Also it can
Dipankar Ray
doaj  

Familial intestinal malrotation and cleft lip and palate: A case report

Journal of Pediatric Surgery Case Reports
Introduction: The etiology of intestinal malrotation is unknown and it can occur in isolation or with other congenital anomalies. Although case reports have reported genetic etiologies of intestinal malrotation, association with cleft lip and palate is ...
Kamela Loo, Krista Lai, Vidhi Shah
doaj   +1 more source

Operative approach to intestinal malrotation encountered during laparoscopic gastric bypass

Journal of Surgical Case Reports, 2020
Congenital anomalies of midgut rotation are uncommon with a 0.2–0.5% incidence. Intestinal malrotation (IM) presents a unique challenge in bariatric surgery during laparoscopic gastric bypass (LRYGB), and familiarity with alternatives allows for safe ...
Nicole Shockcor, R. Nzara, Anam Pal, E. Lo Menzo, M. Kligman   +4 more
semanticscholar   +1 more source