What should I do if I have the spinal muscular atrophy gene but do not have SMA?

If you have been diagnosed as a carrier of the SMA gene but are not affected by the condition, you should still seek the advice of a genetic counselor or your doctor. This is very important if you are considering having a child. He or she will be able to help you evaluate your risks and chances of having a child with spinal muscular atrophy. If you have already had a child with SMA, your counselor should be able to advise you of your options regarding future pregnancies.

Resources

Cure SMA

925 Busse Road

Elk Grove Village, IL 60007

800.886.1762

Fax: 847.367.7623

info@fsma.org www.curesma.org

Muscular Dystrophy Association

National Office - 222 S. Riverside Plaza Suite 1500

Chicago, IL 60606

800.572.1717

Fax: 520.529.5300

mda@mdausa.org www.mda.org

Fight SMA

1321 Duke Street Suite 304

Alexandria, VA 22134

703.299.1144

web@fightsma.org www.fightsma.org

Spinal Muscular Atrophy Foundation

888 Seventh Avenue, Suite 400

New York, NY 10019

877.FUND.SMA (877.386.3762), 646.253.7100

Fax: 212-247-3079

info@smafoundation.org

www.smafoundation.org

Last reviewed by a Cleveland Clinic medical professional on 11/24/2015.

References

  • Darras BT, Markowitz JA, Monani UR, De Vivo DC. Spinal muscular atrophies. In: Darras BT, Jones HR, et al, editors. Neuromuscular Disorders of Infancy, Childhood, and Adolescence. 2nd ed. Amsterdam: Academic Press, an imprint of Elsevier; 2014: Chap 8.
  • Amato AA, Russell JA. Spinal Muscular Atrophies. In: Amato AA, Russell JA. eds. Neuromuscular Disorders, 2e. New York, NY: McGraw-Hill; 2015.
  • Genetics Home Reference. Spinal muscular atrophy Accessed 11/24/2015.
  • National Human Genome Research Institute. Learning About Spinal Muscular Atrophy Accessed 11/24/2015.
  • Muscular Dystrophy Association (MDA). Spinal muscular atrophy Accessed 11/24/2015.

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