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A novel case report of spinal muscular atrophy with progressive myoclonic epilepsy from Iran
Spinal muscular atrophy (SMA) is a disorder characterized by decreased motor function due to the muscle atrophy in the background of degenerated anterior horn cells and motor cells of lower cranial nerves nuclei. The most frequent form is inherited as an autosomal recessive trait resulting from muta...
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| Publicado no: | Int Med Case Rep J |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6549484/ https://ncbi.nlm.nih.gov/pubmed/31213928 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IMCRJ.S202046 |
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