![]() Rhabdomyolysis can result from inherited muscle disorders, infections and an internal deficiency of muscle enzymes, often manifest in childhood.Īlthough, another characteristic would change my response in as follow ways. Besides, the causes of rhabdomyolysis may be metabolic myopathies – a group of hereditary diseases, the leading symptom of myoglobinuria. The predisposing environment includes factors contributing to the corresponding genetic characteristics (McCane & Huether, 2019). However, the human genotype is the background on which they act and can strengthen or weaken the influence of other factors in the development of addictions. The nature of this phenomenon is diverse, and in each particular case, it may be the result of the influence of various factors. Most geneticists agree that there is a significant role in developing a genetic predisposition to dependence on harmful substances. The subsequent release of intracellular ions, myoglobin, creatine kinase, and urates into the bloodstream leads to electrolyte disturbances, disseminated intravascular coagulation, renal failure, and multiple organ failure. It is a clinical syndrome in which skeletal muscle tissue is destroyed. ![]() Such disease is evidenced by an increased level of potassium in the blood serum, as well as necrotic tissues (McCance & Huether, 2019). The patient’s complaints, the evaluation in the ED, and the conducted EKG method indicate the symptoms and signs of rhabdomyolysis. 308 qualified specialists online Learn more
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