Results 31 to 40 of about 4,757 (204)
Rhabdomyolysis Episode in an Individual with McArdle’s Disease after Low Aerobic Exercise
Saudi Journal of Kidney Diseases and Transplantation, 2022 McArdle’s disease, known as blockage of muscle glycogen metabolism, is characterized by glycogen accumulation of chains in skeletal striated muscles. One of the typical symptoms of the disease is the feeling of intolerance to exercise. Severe muscle cram
Guilherme Henrique Mattos Dantas +6 more
doaj +1 more source
Severe Rhabdomyolysis Associated with Acute Amphetamine Toxicosis in a Dog
Case Reports in Veterinary Medicine, 2020 A 3-year-old female spayed rat terrier presented for hyperactivity and repetitive circling to the right of less than one-hour duration. On examination, the patient was dehydrated, hyperactive, and dysphoric. Laboratory tests initially revealed elevations
M. Ryan Smith, Virginie A. Wurlod
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, 2010 Metadata assigned by Dr. M. van Schoor, Senior Lecturer, Dept. of Companion Animal Clinical StudiesDESCRIPTION: Myoglobinuria is the presence of myoglobin in urine and causes the urine to turn dark red to brown or even black in severe cases ...
John Vissing
core +2 more sources
Rhabdomyolysis in water buffaloes (Bubalus bubalis)
Brazilian Journal of Veterinary Pathology, 2019 Rhabdomyolysis is a myopathy characterized by severe acute myonecrosis with lysis of muscle cells and extravasation of its content into the bloodstream, causing a secondary renal failure and myoglobinuria.
Ignacio Llada +7 more
doaj +1 more source
Clinical and literature review of a case of myopathic form of carnitine palmitoyltransferase Ⅱ deficiency [PDF]
精准医学杂志Objective To explore the correlations of genotype and phenotype of myopathic form of carnitine palmitoyltransferase Ⅱ (CPT Ⅱ) deficiency and to improve the clinical understanding of the disease.
LU Guangshuang, XIA Mingnong, CHENG Yun, HU Jie, LI Wenbo, ZHANG Fan, YANG Wu
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Molecular Genetics and Metabolism Reports, 2021 A 29-year-old man developed, since the age of 18, exercise intolerance and exercise-induced rhabdomyolysis, with myoglobinuria. Muscle biopsy showed ragged-red fibers. Multiple mitochondrial DNA deletions were detected. The previously reported pathogenic
Carlos Pablo de Fuenmayor-Fernández de la Hoz +7 more
doaj +1 more source
Veterinary Dermatology, EarlyView.Background: Oclacitinib is a Janus kinase inhibitor approved for the treatment of pruritus associated with allergic dermatitis in dogs and may be effective in horses. Objectives: To evaluate the efficacy of oclacitinib in reducing pruritus and skin lesions in horses with allergic dermatitis.
Nuttawut Nuchprayoon +6 more
wiley +1 more source
Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathy
, 2014 Myoglobinuria is a frequent complication of metabolic myopathies and may also occur in Duchenne and Becker dystrophies but is not a typical sign of limb-girdle muscular dystrophy.
Rodolico, Carmelo +4 more
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McArdle’s disease: A case of exercise intolerance and myopathy
Journal of Dr. NTR University of Health SciencesMcArdle disease is a hereditary glycogen storage disorder caused by a deficiency in the enzyme myophosphorylase, leading to impaired glycogen breakdown in skeletal muscles.
Prince Saha +2 more
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Clinical Genetics, Volume 110, Issue 1, Page 15-28, July 2026.Advances in genomic, proteomic, and transcriptomic technologies are transforming the diagnosis of genetic myopathies. When integrated with traditional muscle pathology, multi‐omics approaches improve diagnostic yield, clarify disease mechanisms, and support more precise, mechanism‐based therapeutic strategies for patients with neuromuscular disorders ...
Ludmila Alem +2 more
wiley +1 more source