Spinal muscular atrophy, genetic and molecular SMA Cases

Spinal muscular atrophy, genetic and molecular discoveries and on future prospects for the treatment of spinal muscular atrophy SMA Cases. Quick diagnosis and provide appropriate and timely support. Information collected from scientific articles, retrieved from databases.

SMA Is neurodegenerative disorder with autosomal recessive genetic heredity, SMN protein survival motor Neuron SMN1. This genetic alteration results in reduced levels of the SMN Protein cases. basic nutritional and respiratory care and physiotherapy basic treatment

Spinal muscular atrophy, motor neuron, therapy all services, Autosomal recessive heredity genetic alteration to the SMN1 gene is responsible for a reduction for everyone.