Clinical Diagnosis of Rhabdomyolysis without Myoglobinuria or Electromyographic Abnormalities in a Dog [PDF]
Animals, 2023 A 2-year-old female neutered Old German Shepherd was presented for acute non-ambulatory tetraparesis. Upon presentation to the emergency department, hematology and biochemical blood tests revealed no abnormalities aside from mildly elevated C-reactive ...
Koen Maurits Santifort +2 more
doaj +5 more sources
Spread of alimentary-toxic paroxysmal myoglobinuria-haff disease (literature review) [PDF]
E3S Web of Conferences, 2021 In 1924, Haff disease was first detected in East Prussia. Till now, cases of Haff disease have been recorded in Sweden, Russia, the United States, China, Brazil, Japan, and China among people and animals.
Glazunova L.A. +4 more
doaj +3 more sources
Primary Myoglobinuria: Differentiate Myoglobinuria from Hemoglobinuria [PDF]
Indian Journal of Clinical Biochemistry, 2016 Myoglobin is dark red colour heme containing protein, stored in muscle. Change in permeability of myolemma causes myoglobin leak in plasma, which is cleared by kidney swiftly. Differentiating myoglobinuria from hemoglobinuria is important. Clinicians concern over myoglobinuria is to protect the patient from acute renal disease.
exaly +3 more sources
Athletic pseudonephritis in male cross-country ultra-marathoners: a comparative observational study [PDF]
Frontiers in PhysiologyBackground/ObjectiveAthletes have commonly reported hematuria, cylindruria, and proteinuria, which are consistent with “athletic pseudonephritis.” To date, little is known about the overall consequences of 100 km (62.5-mile) cross-country ultra-marathons
Kai-Hung Chen +22 more
doaj +2 more sources
Severe falciparum malaria with dengue coinfection complicated by rhabdomyolysis and acute kidney injury: an unusual case with myoglobinemia, myoglobinuria but normal serum creatine kinase [PDF]
BMC Infectious Diseases, 2012 Background Acute kidney injury (AKI) is a complication of severe malaria, and rhabdomyolysis with myoglobinuria is an uncommon cause. We report an unusual case of severe falciparum malaria with dengue coinfection complicated by AKI due to myoglobinemia ...
Yong Kok Pin +2 more
doaj +3 more sources
Dermatomyositis presenting with rhabdomyolysis and acute renal failure; an uncommon manifestation [PDF]
Annals of Indian Academy of Neurology, 2009 Rhabdomyolysis and myoglobinuria are a rare complication of dermatomyositis. Such patient can land up in acute renal failure. Recognition of this fact has important therapeutic implications as patients require immunotherapy in addition to the symptomatic
Joshi Deepika, Kumar Niraj, Rai Anand
doaj +1 more source
Pigment cast nephropathy; time to revisit the diagnosis [PDF]
Journal of Nephropathology, 2021 Pigment cast nephropathy is one of the most severe complications of rhabdomyolysis. It is an important cause of renal failure requiring renal replacement therapy.
Ahmed Waheed Kashif +2 more
doaj +1 more source
Downer cow syndrome causing rhabdomyolysis and acute renal failure in a 17-month-old Guzerá heifer
Ciência Rural, 2021 : The downer cow syndrome (DCS) is characterized by an alert cow showing inability or reluctance to stand for 12 hours or more. This paper reported clinical, laboratory, and pathological findings in a Guzerá heifer with rhabdomyolysis, pigmenturia and ...
Teresa Souza Alves +9 more
doaj +1 more source
Postoperative Malignant Hyperthermia-A Medical Emergency: A Case Report and Review of Literature [PDF]
Journal of Clinical and Diagnostic Research, 2017 Malignant hyperthermia is a rare life threatening pharmacological disorder. Preoperative clinical diagnosis is not possible. Due to its rarity and severity, it must be taken as an important differential diagnosis for postoperative hyperthermia.
Amit Kumar Sinha +4 more
doaj +1 more source
Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the ACADVL Gene
Brain Sciences, 2023 Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a rare autosomal recessive long-chain fatty acid oxidation disorder caused by mutations in the ACADVL gene.
Beatrice Labella +9 more
doaj +1 more source