SPONTANEOUS MYOGLOBINURIA: REPORT OF A CASE WITH SYMPTOMS OF MYOTONIA

Abstract
A case is reported of spontaneous myoglobinuria in a patient with symptoms suggestive of myotonia congenita. Spectroscopic examination of the urine showed adsorption bands characteristic of metmyoglobin and oxymyoglobin. The patient''s symptoms related to the myoglobinuria were mild and the patient was able to continue working.

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