Understanding this topic
Duchenne muscular dystrophy (DMD) is a genetic condition causing progressive muscle weakness due to absent or severely reduced functional dystrophin. It commonly affects boys, although girls and women with DMD gene variants can have muscle or heart symptoms.
What families should know
DMD is usually inherited in an X-linked pattern, but a genetic variant may also arise without a known family history.
Medical notice: This information is educational and is not individualized medical advice. Consult a neuromuscular specialist.
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What is Duchenne muscular dystrophy? →Early signs and symptoms →Diagnosis and testing →Genetics and inheritance →Treatments and care options →Heart health in Duchenne →Breathing and respiratory care →Living with Duchenne →Building a Duchenne care team →Clinical trials and research →Frequently asked questions →Trusted Duchenne resources →Editorial standards →About DuchenneGuide →
Further reading
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