Results 231 to 240 of about 852,230 (302)

Suspected Pentalogy of Cantrell With Ectopia Cordis in a Newborn: Diagnostic and Management Challenges in a Low Resource Setting in Northern Tanzania

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Suspected Pentalogy of Cantrell with ectopia cordis carries very high neonatal mortality. In low‐resource settings, absent antenatal ultrasound and limited access to imaging and pediatric cardiac surgery reduce diagnostic certainty and survival.
Tabitha Mshanga   +3 more
wiley   +1 more source

Rapid Progression of Acute Acalculous Cholecystitis to Gangrenous Cholecystitis in an Initially Non‐Critically Ill Patient: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Acute acalculous cholecystitis (AAC) is not confined to the critically ill and may behave like calculous disease. A 65‐year‐old hypertensive man with localized, stone‐free cholecystitis deteriorated on hospital Day 4 with peritonism, acidosis, and acute kidney injury.
Rami Y. Adam   +5 more
wiley   +1 more source

Severe and Enduring Eating Disorders: A Qualitative Study of Patients' Experiences and Perceived Treatment Needs

open access: yesEuropean Eating Disorders Review, Volume 34, Issue 6, Page 1454-1464, November 2026.
ABSTRACT Objective Approximately 25% of individuals with eating disorders develop severe and enduring eating disorders (SEEDs); yet effective treatments remain limited. This study explored lived experiences of SEEDs, focussing on past treatments, as well as current needs and hopes. Method Twenty participants with eating disorders of ≥ 7 years and prior
Emilia Kotilahti   +3 more
wiley   +1 more source

Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency

open access: yesJournal of Inherited Metabolic Disease, Volume 49, Issue 6, November 2026.
ABSTRACT Primary pyruvate dehydrogenase complex deficiency (PDCD) comprises a group of monogenic disorders caused by pathogenic variants in genes encoding subunits of, or regulatory components affecting, the pyruvate dehydrogenase complex. The clinical phenotype spans a broad continuum, ranging from early onset congenital lactic acidosis to infantile ...
Nandaki Keshavan   +23 more
wiley   +1 more source

Gastroschisis‐Like Defect in a Crossbred Bovine Calf: Anatomical, Clinical and Surgical Perspectives

open access: yesVeterinary Medicine and Science, Volume 12, Issue 6, November 2026.
A gastroschisis‐like defect was observed in a one‐day‐old, crossbred bovine calf with evisceration of the pyloric abomasum and small intestine, likely resulting from prenatal rupture of an omphalocele. The calf presented with lethargy, hypothermia and metabolic derangements, along with elevated renal biomarkers.
Mohammad Raguib Munif   +1 more
wiley   +1 more source

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