Results 61 to 70 of about 4,013 (133)
Encephalic xanthomas in a large malayan chevrotain (Tragulus napu)
An adult water chevrotain was euthanized due to severe non-responsive pododermatitis. Incidentally, multiple to coalescing cholesterol granulomas were identified within the right diencephalon, characterized by the presence of foamy macrophages and ...
María F. González +3 more
doaj +1 more source
Key Clinical Message Managing diabetic ketoacidosis (DKA) in individuals with severe dyslipidemia necessitates a comprehensive approach. While rehydration and continuous insulin infusion are fundamental components of DKA management due to the underlying ...
Ankit Shrestha +4 more
doaj +1 more source
Endoscopic appearance of esophageal xanthoma
Background and study aims Esophageal xanthomas are considered to be rare, and their endoscopic diagnosis has not been fully elucidated. The aim of the present study was to determine the characteristics of the endoscopic appearance of esophageal xanthomas.
Kenta Hamada +22 more
doaj +1 more source
The first in this series of historical reviews dealt with the pioneering animal model work of Anitschkow, implicating blood cholesterol in the pathogenesis of atherosclerosis, and the pivotally important work of Gofman, providing evidence that ...
Daniel Steinberg
doaj +1 more source
Diffuse plane xanthomatosis in a patient with Budd-Chiari syndrome and monoclonal gammopathy
Diffuse plane xanthomas are characterized by the presence of yellowish plaques on the eyelids, neck, upper trunk, buttocks, and flexural folds. Histology shows foamy histiocytes in the dermis.
Kocak Mukadder +4 more
doaj
Homozygous familial hypercholesterolemia: A rare case report
A 9-year-old male child presented with asymptomatic skin-colored-to-yellowish nodules over both the buttocks, feet, and over the right Achilles' tendon for 4 years.
Shashikant Malkud +3 more
doaj +1 more source
Aim. To identify character and prevalence of apolipoprotein (apo) B-100 gene mutation in patients with clinical diagnosis of heterozygote familial hypercholesterolemia (FH); to describe its phenotypical features in mutation carriers. Material and methods.
P. P. Malyshev +3 more
doaj
Familial hypercholesterolemia revealed by multiple xanthomas
Familial hypercholesterolemia (HF) is a rare pathology characterized by a major elevation of LDL associated with tendinous and subcutaneous xanthomas. We report the case of a 16-year-old patient, born from a first degree consanguineous marriage, with no ...
Nassiba Elouarradi, Nawal El Ansari
doaj +1 more source
Early-Onset Myocardial Infarction in a 13-Year-Old With Homozygous Familial Hypercholesterolemia Managed by PCI. [PDF]
Siddiqui FI +7 more
europepmc +1 more source
Atherosclerosis at Warp Speed: The Urgent Lessons of Homozygous Familial Hypercholesterolemia. [PDF]
Drossner D.
europepmc +1 more source

