Spinal Muscular Atrophy (SMA)
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What is spinal muscular atrophy? Spinal muscular atrophy (SMA) represents a group of genetic (inherited) neuromuscular disorders that cause certain muscles to become weak and waste away (atrophy). SMA involves the loss of a specific type of nerve cell in your spinal cord called lower motor neurons, or anterior horn cells. These cells control muscle movement. Without these motor neurons, muscles don’t receive the nerve signals that make them move. The weakness in SMA tends to be more severe in th
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While newborn screening will catch most cases of spinal muscular atrophy, children born prior to the advent of newborn screening can present with symptoms later in life. In this video, Dr. Crystal Proud, director of neurology at #CHKD, discusses symptoms that warrant a referral to a neuromuscular neurologist and treatment options that are changing lives and history of spinal muscular atrophy. #NewbornScreening #SpinalMuscularAtrophy | Children's Hospital of The King's Daughters (CHKD)
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