Simple Facts About Spinal Muscular Atrophy

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by Wendy Henderson |

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In this short animated video from Julia Brownholtz shared in January 2015, we find out some basic information about spinal muscular atrophy (SMA), a rare genetic disease which affects around one in 10,000 babies and the number one fatal disease for infants.

Read about five experimental therapies for SMA you might find interesting. 

The video explains what the symptoms of the disease are, why it happens, who discovered the condition and what the progression of spinal muscular atrophy is. Julia explains which faulty gene is responsible for SMA, and how one in 50 Americans carry the faulty SMN1 gene.

Better understand the mechanisms of spinal muscular atrophy with this animated film.

SMA News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.