Duchenne Muscular Dystrophy- Patient UK Website | DuchenneXchange

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Duchenne Muscular Dystrophy- Patient UK Website

key information

source: Patient Info

authors: Dr Colin Tidy

summary/abstract:

Duchenne muscular dystrophy is a condition which causes muscle weakness. It starts in childhood and may be noticed when a child has difficulty standing up, climbing or running. It is a genetic condition and can be inherited. It usually affects only boys, although girls may carry the Duchenne gene. Boys with Duchenne muscular dystrophy should have regular check-ups and physiotherapy from childhood. They are likely to need increasing help and treatments from about the age of 9 years.

DMD is an inherited (genetic) condition which affects the muscles, causing muscle weakness. It is a serious condition which starts in early childhood. The muscle weakness is mainly in the ‘proximal’ muscles, which are those near the trunk of the body, around the hips and the shoulders. This means that fine movements, such as those using the hands and fingers, are less affected than movements like walking.

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