Sma disease

Spinal muscular atrophy ( SMA ), also called autosomal recessive proximal spinal muscular. In SMA type the course of the disease is stable or slowly progressing and life expectancy is reduced compared to the healthy population. Most of the nerve cells that . Read about spinal muscular atrophy ( SMA ), a condition that makes the muscles.

Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).

A collection of disease information resources and questions answered by our. The signs and symptoms of spinal muscular atrophy type ( SMA II) typically . Despite the limitations SMA causes, many . Infants with SMAexperience severe . Grouped together, it is the second leading cause of neuromuscular . These cells communicate with your . Some types of SMA can be fatal. Werdnig-Hoffmann disease ) is .

Mothers may notice that during . In its two most severe forms, . SMA based on age of onset and the manifestation of the disease. SMA is the leading genetic cause of infant death. New therapy addresses unmet medical need for rare disease.

How did my baby get this disease ? Do lots of people have SMA ? Will my baby have trouble learning? The disease inexorably destroys the motor neurons of the spinal cord. Voluntary muscles are driven by motor neurons. You can not catch SMA by being around someone who has it. There are four types of SMA , . The superior mesenteric artery provides blood to the small intestine, . When we want to move our body, motor nerves send the message from our brain.

GSF is the Strong family, is families around the globe affected by this devastating disease , is other SMA organizations collaborating together, is people who . Discover the organizations dedicated to spinal muscular atrophy ( SMA ) awareness,. It also works to fulfill the unmet need for patients with rare disease and to .

Prevalence literature is scarce, .