McArdle disease is a rare myopathy caused by hereditary myophosphorylase deficiency. It presents nonspecific symptoms, such as intolerance to physical exercise, early fatigue, and myalgias, and represents a paradigmatic example of one of the main challenges in clinical practice: the recognition of nonspecific and common symptoms as clinically relevant manifestations of rare diseases. The nonspecificity of symptoms leads to a frequent delay from the onset of first clinical signs to diagnosis. We present a case of McArdle disease diagnosed in a Portuguese adult patient. We believe this report will highlight the need to enhance knowledge and awareness about this rare pathology to diagnose and manage these patients promptly.
Keywords: glycogen storage disease type v; mcardle disease; myalgias; myophosphorylase deficiency; rhabdomyolysis.
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