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Clinical Trial Summary

Spinal muscular atrophy (SMA) is an autosomal recessive disease that causes progressive muscle wasting and weakness due to loss of motor neurons in the spinal cord. This is a registered cohort of spinal muscular atrophy (SMA) type I,II and III in China. This study will provide further insights into the clinical course of SMA including overall survival, demographic characteristics, motor function, respiratory support, feeding and nutritional support, growth and development. The correlation of genotype and phenotype will be conducted.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04010604
Study type Observational
Source First Affiliated Hospital of Fujian Medical University
Contact Yi Lin, PhD
Phone 86-0591-87982772
Email linyi7811@163.com
Status Recruiting
Phase
Start date July 1, 2019
Completion date December 31, 2049

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