Phosphoglycerate Mutase Deficiency

While permanent weakness is rare with this genetic enzyme deficiency with onset in childhood and early adulthood, exercise intoelerance, cramps, muscle pain,and sometimes rust colored urine, which indicates muscle breakdown, makes avoiding intense exercise advisable to avoid permanent muscle tissue damage. This disease is autosomal recessive, caused by the contribution of a defective gene from each parent.

There are no listings in this category.
Search for in

submit Category Stats
Listings: 0