Duchenne muscular dystrophy (Q41380): Difference between revisions
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Latest revision as of 07:31, 13 August 2026
Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C70.1 |
||
| English | Duchenne muscular dystrophy |
Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking. |
Statements
CID11:8C70.1
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dki-india-8C70.1
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Concluído
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13 August 2026
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