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Current Neurology and Neuroscience Reports, 2015
One large group of hereditary myopathies characterized by recurrent myoglobinuria, almost invariably triggered by exercise, comprises metabolic disorders of two main fuels, glycogen and long-chain fatty acids, or mitochondrial diseases of the respiratory chain. Differential diagnosis is required to distinguish the three conditions, although all cause a
BARCA, EMANUELE +2 more
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One large group of hereditary myopathies characterized by recurrent myoglobinuria, almost invariably triggered by exercise, comprises metabolic disorders of two main fuels, glycogen and long-chain fatty acids, or mitochondrial diseases of the respiratory chain. Differential diagnosis is required to distinguish the three conditions, although all cause a
BARCA, EMANUELE +2 more
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, 2006 Neurologic Clinics, 2000
Myoglobinuria refers to an abnormal pathologic state in which an excessive amount of myoglobin is found in the urine, imparting a cola-like hue, usually in association with myonecrosis and a clinical picture of weakness, myalgias, and edema. Myoglobinuria is produced by multiple causes: any condition that accelerates the use or interferes with the ...
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Myoglobinuria refers to an abnormal pathologic state in which an excessive amount of myoglobin is found in the urine, imparting a cola-like hue, usually in association with myonecrosis and a clinical picture of weakness, myalgias, and edema. Myoglobinuria is produced by multiple causes: any condition that accelerates the use or interferes with the ...
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IDIOPATHIC PAROXYSMAL MYOGLOBINURIA
Pediatrics, 1959A case of idiopathic paroxysmal myoglobinuria is reported. This is a disease of unknown etiology, characterized by severe muscle pain and weakness or complete paralysis and by the excretion of burgundycolored urine. The urine is free of erythrocytes but gives a strongly positive benzidine reaction. There is no discoloration of the plasma.
G W, DAUGHERTY +2 more
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Influenza and myoglobinuria in brothers
Neurology, 1979Two adult brothers became ill within 48 hours of each other, and both had severe myoglobinuria. One brother died of oliguric renal failure. The other did not have renal failure and survived. Acute influenza A infection was documented serologically and from throat washings in the surviving brother, and by isolation of the influenza A virus from throat ...
K, Zamkoff, N, Rosen
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Military Concern with Myoglobinuria
Annals of Internal Medicine, 1972Excerpt To the editor: As indicated by Hamilton and associates in their July 1972 article (p. 77) on exercise-induced myoglobinuria, the syndrome of acute exertional rhabdomyolysis is of particular...
E L, Gitin, M A, Demos, J F, Adams
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Severe dystonia and myoglobinuria
Neurology, 1982Myoglobinuria may follow extreme muscular exertion or disorders that cause muscle necrosis. Dystonia has not been implicated previously. We studied an 8-year-old boy of non-Jewish, Mexican-American descent with autosomal-dominant dystonia musculorum deformans who developed rapidly progressive and severe generalized dystonia, hyperpyrexia, myoglobinuria,
J, Jankovic, A S, Penn
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IDIOPATHIC PAROXYSMAL MYOGLOBINURIA
Journal of the American Medical Association, 1960Acute attacks of muscle pain occasionally so severe as to cause pseudoparalysis, associated with the appearance of myoglobin in the urine, and due to an unrecognizable cause have been given various names of which the most frequently used is idiopathic paroxysmal myoglobinuria. We have been able to find only 37 cases reported in the medical literature.
P J, PHILLIPPI, F R, JONES, W L, KENOYER
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