Common "Mcardle's Disease" queries answered by top doctors | iCliniq

Mcardle's Disease

Mcardle's disease is one of the types of glycogen storage disease. It is a rare genetic muscular disorder that results due to the inability of the muscle cells to break down glycogen into sugar for energy. This condition causes muscle pain and tiredness during exercise and can lead to dark urine.

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What is McArdle's disease?

Query: Hello doctor, My brother has done a McArdle's test in hospital. They concluded that the glycolysis in cytoplasm is normal, but reduced function of mitochondriosis have been seen in muscle. They conclude this abnormality through the blood analysis. The respiratory and the cardiac functions have been ...  Read Full »


Dr. Puneet Kumar Bansal

Answer: Hi, Welcome to icliniq.com. McArdle's disease is caused by deficiency of enzyme glycogen phosphorylase, which causes inability to breakdown glycogen. It is a genetic disease; autosomal recessive, which means when both your parents have abnormal gene it is inherited. Just you have to vary dietary ha...  Read Full »

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