Results 41 to 50 of about 682,260 (169)

Fetal malrotation with midgut volvulus: Prenatal diagnosis and planning

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Malrotation of the intestinal tract is a congenital malformation commonly found either incidentally or after affected individuals develop signs and symptoms of intestinal obstruction.
Oluyinka O. Olutoye II, J.D. Hammond II, Jamie Gilley, Ross M. Beckman, Marie Bulathsinghala, Sonya S. Keswani, Jonathan Davies, Mark V. Mazziotti, Roopali Donepudi, Michael A. Belfort, Alice King, Pamela M. Ketwaroo, Timothy C. Lee   +12 more
doaj   +1 more source

Laparoscopic Surgery for Colon Cancer with Intestinal Malrotation: A Case Report and Review of the Literature in Japan

, 2021
Colorectal cancer with intestinal malrotation is very rare, while intestinal malrotation is one of congenital anomaly that is rare in adults. We thus report a case of sigmoid colon cancer with intestinal malrotation treated by laparoscopic surgery.
Manabu Yamamoto, K. Sakata, H. Yano, T. Gion, Y. Tominaga, Hiroyuki Kobayashi, M. Tuneyoshi   +6 more
semanticscholar   +1 more source

Duplication cyst mimicking intestinal malrotation with volvulus: A case report

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Neonates presenting with bilious vomiting require emergent evaluation to rule out malrotation with volvulus. Enteric duplication cysts are congenital gastrointestinal lesions that can cause intestinal obstruction.
Matthew Ballweg, Patrick B. Thomas, Abdalla Zarroug, Angela, M. Hanna   +3 more
doaj   +1 more source

Diagnostic Challenges in Adult Intestinal Malrotation: A Case Report and Literature Review

Cureus
Adult intestinal malrotation is a rare anatomical anomaly that typically manifests during infancy but can also present in adulthood. Symptoms are mainly digestive, with a long history of intermittent abdominal pain and epigastralgia.
Chirwa Abdillahi Mahamoud, Abdoulrazak Egueh Nour, N. Bouknani, Najwa Benslima, A. Rami   +4 more
semanticscholar   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Waugh syndrome: A rare coexistence of intussusception and intestinal malrotation: Case report and literature review

International journal of surgery case reports
Introduction Waugh's syndrome, characterized by the concurrent presence of acute intussusception and gut malrotation, is a rare clinical entity. The relationship between these conditions is not well-explored, and the true incidence may be underreported ...
Malvina Asbah, Oadi N. Shrateh, Hadeel Ashqar, Asil Musleh, Khaled Abbadi, Wael Amro   +5 more
semanticscholar   +1 more source

Hirschsprung disease and intestinal malrotation: A rare association with unique perioperative considerations

Journal of Pediatric Surgery Open, 2023
Background: Multiple etiologies exist for neonatal intestinal obstruction with similar presenting symptoms. While single etiology is the most common cause, concomitant surgical diagnoses exist requiring unique peri‑operative considerations.
Dimitra M. Lotakis, Sydni Imel, Jack P. Vernamonti, Brianna L. Spencer, Matthew W. Ralls   +4 more
doaj   +1 more source

Febrile status epilepticus and epileptogenesis: The FEBSTAT study

Epilepsia Open, EarlyView.
Abstract The multicenter FEBSTAT study (Consequences of Prolonged Febrile Seizures in Childhood: https://grantome.com/grant/NIH/R37‐NS043209‐12; PI S. Shinnar) examined the outcome of febrile status epilepticus (FSE) in over 200 prospectively enrolled infants, with many followed for 10 years after FSE.
Darrell V. Lewis, Douglas R. Nordli Jr., Douglas R. Nordli III, Shlomo Shinnar, Stephen Chan, Jacqueline A. Bello, L. Matthew Frank, James Voyvodic, William Gallentine, Syndi Seinfeld, Yoshimi Sogawa, Erica Weiss, David Masur, Yuan Xu, Solomon L. Moshé   +14 more
wiley   +1 more source

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea

JPGN Reports, EarlyView.
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno, Angelo Corso Faini, Silvia Deaglio, Marianna Pellegrini, Raffaele Buganza, Francesca Giuliani, Pier Luigi Calvo, Michele Pinon   +7 more
wiley   +1 more source

Case Report: Ultrasound “whirlpool sign” in fetal intestinal malrotation and torsion: a case-based approach to early diagnosis and intervention

Frontiers in Pediatrics
IntroductionFetal ascites is a rare condition that may indicate underlying gastrointestinal malformations, including congenital intestinal malrotation.
Yueyun Liu, Rongjie Zheng, Zonghua Liu, Jun Zhou   +3 more
doaj   +1 more source