Results 71 to 80 of about 15,349 (197)

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

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
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   +4 more
wiley   +1 more source

A case of perforation of Meckel’s diverticulum with enterolith

open access: yesSurgical Case Reports, 2020
Background Perforation of Meckel’s diverticulum with enteroliths is a rare complication. Here, we report a case of perforation of Meckel’s diverticulum with one enterolith, which could not be accurately diagnosed by preoperative computed tomography. Case
Tomonari Shimagaki   +11 more
doaj   +1 more source

Meckel's Diverticulum Enterolith : A Rare Cause of Acute Abdomen

open access: yes, 2009
Meckel's diverticulum (MD) is the most common congenital anomaly of the gastro-intestinal tract. Inflammation, bleeding and obstruction are its main complications. Formation of enterolith is rare. A case of acute abdomen caused by Meckel's diverticulitis
Agaoglu, N.
core   +1 more source

Essential embryology for the Canadian pathologists’ assistant

open access: yesAnatomical Sciences Education, Volume 19, Issue 7, Page 1134-1156, July 2026.
Abstract Pathologists' assistants (PAs) are pivotal in healthcare, conducting autopsies and examining tissues under a pathologist's guidance. Embryology knowledge is crucial for PAs to accurately assess anomalies and identify pathologies. Yet, it is often overlooked in academic PA training programs.
Samantha H. Nacci   +4 more
wiley   +1 more source

Meckel’s Diverticulum: Prevalence in 1000 Laparatomies [PDF]

open access: yesPatient Safety and Quality Improvement Journal, 2013
Objectives: To detect the prevalence of Meckel's Diverticulum in children and adults aged 1 day to 90 years old. Materials and Methods: This is a cross sectional descriptive study of 1000 cases aged 1 day to 90 years old in the surgery wards of two ...
Bazrafshan A, Heydarian F, Rahmani Sh
doaj  

Perforation of the Meckel’s diverticulum with a chicken bone: a case report and literature review

open access: yesSurgical Case Reports, 2019
Background Meckel’s diverticulum (MD) is the most common congenital abnormality of the gastrointestinal (GI) tract. Most of the people remain asymptomatic during their lifetime, but some can develop complications such as inflammation, haemorrhage or ...
Bardia Bidarmaghz   +3 more
doaj   +1 more source

Effects of Different Levels of Methionine in Liquid and Powder Forms on Growth Performance, Blood Parameters, and Carcass Traits of Broiler Chickens

open access: yesVeterinary Medicine and Science, Volume 12, Issue 4, July 2026.
Broiler chickens fed diets with liquid or combined methionine sources (especially 100‐LM and 50‐LPM) showed improved growth, feed efficiency, breast yield, villus height, and antioxidant status, with reduced serum urea, uric acid, and liver enzymes—demonstrating superior efficiency of liquid methionine supplementation.
Parvin Khosravi   +6 more
wiley   +1 more source

Complications of Meckel's diverticulum

open access: yesJournal of British Surgery, 1976
Abstract This paper reviews the presentation and surgical pathology of 50 Meckel's diverticula encountered in one hospital in a 20-year period. It is concluded that in children with intestinal bleeding or a ‘raspberry tumour’ of the umbilicus a Meckel's diverticulum is usually suspected.
T, Moore, A O, Johnston
openaire   +2 more sources

Jejunal Diverticulosis as a Rare Cause of Severe Obscure Gastrointestinal Bleeding in an Elderly Patient: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Jejunal diverticulosis is a rare cause of obscure gastrointestinal bleeding (OGIB) that can present with life‐threatening hemorrhage. We report a 69‐year‐old male with recurrent melena, severe anemia, and hemodynamic instability requiring multiple transfusions. Upper and lower endoscopy were nondiagnostic, and CT angiography failed to localize
Mahmoud Draidi   +5 more
wiley   +1 more source

Bilateral Gonadoblastoma in a 12‐Year‐Old Girl 4 Years After Wilms' Tumor: A Rare Pediatric Case

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This case of a 12‐year‐old patient who developed bilateral gonadoblastoma 4 years after treatment for Wilms tumor highlights the importance of rigorous, risk‐adapted long‐term surveillance and careful evaluation of incidental gonadal findings, even in asymptomatic patients.
Ahmed Quraish   +4 more
wiley   +1 more source

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