Spinal Muscular Atrophy

Spinal-Muscular-Atrophy

Spinal muscular atrophy (SMA) is a genetic disease that attacks nerve cells, called motor neurons, in the spinal cord. These cells communicate with your voluntary muscles – the ones you can control, like in your arms and legs.

Also called: SMA.

Spinal muscular atrophy (SMA) is a genetic disease that attacks nerve cells, called motor neurons, in the spinal cord. These cells communicate with your voluntary muscles – the ones you can control, like in your arms and legs. As the neurons die, the muscles weaken. This can affect walking, crawling, breathing, swallowing, and head and neck control.

SMA runs in families. Parents usually have no symptoms, but still carry the gene. Genetic counseling is important if the disease runs in your family.

There are many types of SMA. Some of them are fatal. Some people have a normal life expectancy. It depends on the type and how it affects breathing. There is no cure. Treatments help with symptoms and prevent complications. They may include machines to help with breathing, nutritional support, physical therapy, and medicines.

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2 thoughts on “Spinal Muscular Atrophy

  1. Ben Wollman says:

    Good day, my name is Ben Wollman I live in Canada, my son has disease called spinal Muscular atrophy (SMA)Type 3,He is 14 years old,I am wondering if you had any success with treating this particular disease, if you could let me know. Thank you

      • Premilife Customer Care says:

        Dear Ben Wollman
        Thank you for approaching us.
        We have answered your question in a personal email sent to you.
        We hope you found our answer sufficient and that it provided you with the information you were looking for.
        If you have further questions, please feel free contacting us using the Contact Premilife page. We will be happy to assist.
        The Premilife customer service

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