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Unknown glycogenosis associated to dystrophy gene deletion: affected person has a previously undescribed myopathy related to both Becker muscular dystrophy and a glycogen storage disorder of unknown aetiology. Strategies to diagnose glycogen storage diseases embrace historical past and physical examination for associated signs, blood checks for associated metabolic disturbances, and genetic testing for suspected mutations. Advancements in genetic testing are slowly diminishing the need for biops...
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