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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Detalles Bibliográficos
Autores principales: Shervin Badv, Reza, Nilipour, Yalda, Rahimi-Dehgolan, Shahram, Rashidi-Nezhad, Ali, Ghahvechi Akbari, Masood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549484/
https://www.ncbi.nlm.nih.gov/pubmed/31213928
http://dx.doi.org/10.2147/IMCRJ.S202046

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549484/
https://www.ncbi.nlm.nih.gov/pubmed/31213928
http://dx.doi.org/10.2147/IMCRJ.S202046

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