Duchenne muscular dystrophy is an inherited muscle disease that usually becomes apparent in early childhood and subsequently leads to muscle weakness.

Due to its X-linked inheritance, it almost exclusively affects boys. It is found in about one in 3,500 newborn boys.

The genetic defect and the resulting impaired dystrophin production are already effective at birth; at this time, a strongly increased creatine kinase activity can be detected in the blood of affected male children. The two types, Duchenne and Becker, differ in the further clinical manifestation.

In addition to conventional medical treatments and therapies, the literature on frequency therapy also contains supportive frequency lists with different manifestations.

Frequency therapy and Duchenne muscular dystrophy

XTRA:

146,153,522,727.5,787,880,5000

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