New Drug Helps Children with Spinal Muscular Atrophy Walk Again

Spinal muscular atrophy is a rare genetic disorder that frequently leads to early death in kids. However, an experimental drug provided incredible results in a new trial. This drug even enabled several children with the condition to walk again.spinal muscular atrophy

The results of the drug, nusinersen, were so incredible that the trial was cut short in August, as it was unfair and to keep some of kids on placebo.

Scientists believe if the final results of the trial will prove the drug efficiency, they could offer hope for patients with similar conditions, such as Hunrigton’s disease, motor neurone disease, and Alzheimer’s disease.

More information about the trial here.

MediGoo is attending the largest health/medical industry event in Düsseford, Germany. We welcome you to visit our stand at hall 15 booth E55. Welcome, hope to see you there 15E55.