For Duchenne and Becker muscular dystrophies, muscle biopsy may show whether dystrophin, a muscle protein, is missing or abnormal, and DNA testing is used to analyze the condition of the related gene.

This quick alphabetical guide will help you feel more confident when talking about muscular dystrophy with your doctor and loved ones. Muscular dystrophy is the name for a group of genetic diseases ...

Dystrophy is any condition in which a part of the body weakens or wastes away. In muscular dystrophy, the weakness is in the muscles. An inherited genetic mistake prevents the body from making a ...

More than 30 rare muscular dystrophy types cause progressive muscle weakness from inherited gene mutations. Combined, they affect about 1 in 5,000 to 8,000 people. Common subtypes vary by age of onset ...

Physical Examination: A physician experienced in the treatment of neuromuscular disorders can suspect myotonic dystrophy based on the physical examination and interaction with the patient. In most of ...

Muscular dystrophy is a group of more than 30 inherited conditions that cause progressive muscle weakness and loss. Some forms of muscular dystrophy are diagnosed in infancy or childhood, while the ...