Condition: Spinal Muscular Atrophy · Sponsor: Wan-Jin Chen
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.
This description comes directly from the study's public registry record.
Yi Lin, PhD · 86-0591-87982772 · linyi7811@163.com
Wan-Jian Chen, PhD · 86-0591-87982772 · wanjinchen75@fjmu.edu.cn
Always discuss trial participation with your own doctor first.
| Department of Neurology, First Affiliated Hospital Fujian Medical University | Fuzhou, Fujian, China | Recruiting |
Save your interest here for when the public record changes — results posted, or the study's status changes. Email alerts for this study aren't switched on yet.
We keep this only about this public record, and never email you without alerts being switched on. Want it removed at any time? Email hello@eichor.com. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.