Panelists discuss how spinal muscular atrophy is an autosomal recessive genetic disease affecting motor neurons with 3 ...

Spinal muscular atrophy (SMA) is a collection of inherited neuromuscular diseases. Muscle weakness is the main symptom, and this can affect breathing, eating, posture, and movement. Some types can ...

Spinal muscular atrophy (SMA) is a rare genetic condition that impairs a person’s ability to control their muscle movement. Most types of SMA are diagnosed in infants, but the condition ...

Spinal muscular atrophy (SMA) is a rare genetic disorder that causes muscle weakness and disability, typically in young children. Learn about symptoms, diagnosis, treatment options, and support.

Spinal muscular atrophy (SMA) is a group of disorders that causes muscle weakness and wasting. SMA affects approximately, 1 in every 6,000 to 10,000 people. Adult-onset SMA usually happens ...

Investigators say thrombospondin-4 levels were reduced in patients with symptoms of spinal muscular atrophy (SMA), but levels of the protein increased after therapy. Patients aged 2-21 receiving ...

How your spinal muscular atrophy (SMA) changes over time depends on many things, including which of the four types of SMA you have. They’re based on when symptoms first show and the highest ...

Spinal muscular atrophy is a disease that most often strikes babies and young children, making it hard for them to move their muscles. SMA is passed down in families from parents to their children.

Infantile spinal muscular atrophy (SMA) is a neuromuscular disorder affecting infants and children. It can cause muscles to weaken and limit muscle movement.

Daily electrical stimulation of certain nerves in the spinal cord appeared to help three people with spinal muscular atrophy (SMA), an inherited disorder that causes muscles to waste away.

Spinal Muscular Atrophy (SMA) is a rare genetic disorder that affects the motor neurons in the spinal cord, resulting in muscle weakness and progressive loss of movement. SMA is a progressive ...