Suspicion of a teenager with Duchenne disease in the pediatrics department of Sainte Thérèse De Hinche Hospital
<p>Duchenne disease is caused by a deletion of the gene coding for dystrophin. The absence of this protein is responsible for the myonecrosis observed during the evolution of the pathology. It is X-linked recessive which explains its occurrence, especially in boys. The manifestation of the dis...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Journal of Neurology, Neurological Science and Disorders - Peertechz Publications,
2023-07-05.
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| Online Access: | Connect to this object online. |
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