Spinal muscular atrophy (SMA) is an inherited disease that attacks motor neurons, the nerve cells that control our muscles. SMA hits children and adults. Children inherit the gene for SMA from both ...

Spinal muscular atrophy (SMA) is a rare genetic disorder that causes severe muscle weakness. SMA usually affects children, and is typically diagnosed in the first 18 months of life. In its most ...

There’s no cure for spinal muscular atrophy (SMA). But there are treatments. Three medications can help slow down SMA symptoms. In some cases, they may be able to stop the disease from getting worse.

Spinal muscular atrophy (SMA) is a group of serious, progressive diseases that destroys motor neuron cells. SMA treatment aims to reduce symptoms and slow or stop the progression of the disease. SMA ...

Spinal muscular atrophy (SMA) is a severe neurological disease for which there is presently no cure, although current therapies can alleviate symptoms. In the search for better treatment options, ...

Spinal muscular atrophy (SMA) is a genetic disease that causes muscle weakness and wasting, known as atrophy. People with SMA often have difficulties moving, swallowing, sitting up, and sometimes ...

SMA is a genetic condition that impacts motor neurons, leading to muscle weakness that affects essential functions like breathing and movement. Treatments like Spinraza and Zolgensma can help manage ...