Anesthesia management in a patient with very long-chain acyl-Coenzyme A dehydrogenase deficiency
JA Clinical Reports, 2020 Background In a patient with very long-chain acyl-Coenzyme A dehydrogenase (VLCAD) deficiency, metabolism of fatty acids is impaired and a supply of alternative energy is limited when glucose level is insufficient on starvation.
Haruyuki Yuasa +5 more
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Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency [PDF]
, 2006 We report two patients in whom phosphoglycerate mutase (PGAM) deficiency was associated with the triad of exercise-induced cramps, recurrent myoglobinuria, and tubular aggregates in the muscle biopsy.
Oh, S. J. +6 more
core +1 more source
Rhabdomyolysis and acute kidney injury after acupuncture sessions
Saudi Journal of Kidney Diseases and Transplantation, 2014 Rhabdomyolysis is usually caused by muscle injury, drugs or alcohol and presents with muscle weakness and pain. It is characterized by rise in serum creatine kinase, aminotransferases and electrolytes as well as myoglobinuria.
Marios Papasotiriou +3 more
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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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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
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Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation [PDF]
, 2015 The most common clinical phenotype caused by a mtDNA mutation in complex I of the mitochondrial respiratory chain is Leber hereditary optic neuropathy.
Christoffer R. Vissing +13 more
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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
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Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood [PDF]
, 2008 Recurrent episodes of life-threatening myoglobinuria in childhood are caused by inborn errors of glycogenolysis, mitochondrial fatty acid beta-oxidation, and oxidative phosphorylation.
Hubert, Laurence +12 more
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Equine Veterinary Education, EarlyView.Summary Calcium carbonate crystals are commonly observed in equine urine; however, crystalluria without urolith formation rarely results in clinically significant disease. A 4‐year‐old Japanese Sport Horse developed recurrent haematuria accompanied by the presence of numerous angular calcium carbonate crystals. Discontinuing the calcium supplementation
R. Sato +3 more
wiley +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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