Results 141 to 150 of about 52,322 (263)

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1719-1724, July 2026.
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi   +11 more
wiley   +1 more source

First Reported Case of Fulminant Weil's Disease in South Khorasan, Eastern Iran: Diagnostic Challenges in a Non‐Endemic Region and Implications for Military Deployment

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Weil's disease should be considered even in non‐endemic regions when compatible clinical findings are accompanied by relevant exposure history. This case is epidemiologically notable as the first documented report from South Khorasan Province, highlighting the diagnostic challenges of leptospirosis in non‐endemic settings and the potential ...
Zohreh Azarkar   +3 more
wiley   +1 more source

Chronic Spontaneous Coronary Artery Dissection in a Young Woman Managed With Coronary Artery Bypass Grafting: A Case Report With Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Spontaneous coronary artery dissection (SCAD) is an uncommon, non‐atherosclerotic cause of acute coronary syndrome, typically occurring in young to middle‐aged women. Although most cases resolve spontaneously with conservative therapy, a small proportion develop chronic dissections that require revascularization.
Gashaw Solela   +13 more
wiley   +1 more source

Hydralazine-Associated Pericardial Effusion Causing Cardiac Tamponade Without Hypotension. [PDF]

open access: yesJACC Case Rep
Akele O   +6 more
europepmc   +1 more source

The Challenge of Determining the Etiology of Encephalopathy in an Elderly Patient

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Encephalopathy is a heterogeneous clinical syndrome with numerous neurological and systemic etiologies. We report the case of a 67‐year‐old man, a chronic ethanol consumer, admitted with a one‐week history of confusional syndrome. Initial laboratory tests revealed severe hypercalcemia, acute kidney injury, mild anemia, and hyperproteinemia ...
Vlad Alexandru Ionescu   +9 more
wiley   +1 more source

An Asymptomatic Case of Type B Aortic Dissection Developing Type A Dissection During Interfacility Transfer: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
Total arch replacement using a frozen elephant trunk for retrograde type A aortic dissection was effective in excising the intimal tear located in the proximal descending aorta. ABSTRACT During the transfer from a hospital to a tertiary hospital, patients with acute aortic dissection can deteriorate due to aortic rupture or extension of the dissection.
Kayo Sugiyama   +3 more
wiley   +1 more source

Inpatient Outcomes and Complications After Left Atrial Appendage Occlusion in Rural Versus Urban Hospitals in the United States

open access: yesClinical Cardiology, Volume 49, Issue 7, July 2026.
A majority of Left atrial appendage occlusion (LAAO) implantations occurred in urban hospitals. Urban patients had higher rates of overall, major, and pulmonary complications, as well as more discharges to home than rural patients in unadjusted analysis.
Amanda Nguyen   +12 more
wiley   +1 more source

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