Muscular Dystrophy, Duchenne Type (DMD)
Alias:
Duchenne Muscular Dystrophy
Dmd
Muscular Dystrophy, Duchenne
Severe Dystrophinopathy, Duchenne Type
Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
Dystrophy, Muscular, Duchenne Type
Benign Duchenne Muscular Dystrophy
Duchenne Motor Neuron Disease
Muscular Dystrophy Duchenne
Duchenne-Griesinger Disease
Duchenne Type Dystrophy
Basic Information
Medical Symptom
Gene & Mutation
Drugs
Disease Model
References
Muscular Dystrophy, Duchenne Type, also known as duchenne muscular dystrophy, is related to muscular dystrophy, becker type and facioscapulohumeral muscular dystrophy 1, and has symptoms including waddling gait and weakness. An important gene associated with Muscular Dystrophy, Duchenne Type is DMD (Dystrophin), and among its related pathways/superpathways are Cell differentiation - expanded index and miRNA role in immune response in sepsis. The drugs Ramipril and Carvedilol have been mentioned in the context of this disorder. Affiliated tissues include Adipose, Umbilical Cord and skeletal muscle, and related phenotypes are scoliosis and respiratory insufficiency
Basic Information
Inheritance
Age Of Onset
Prevalence
Related Gene
Related Models
Reference
MALACARDS
XL
XLD
Child
1-5/10000
2
39
612
Medical Symptom
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Gene & Mutation
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MGI
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Comparison
Al agent
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