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Spinal Muscular Atrophy (SMA): Types, Symptoms & Treatment
There are four primary types of SMA: 1. Type 1 (severe): About 60% of people with SMA have type 1 , also called Werdnig-Hoffman disease. Symptoms appear at birth or within an infant’s first six months of life. Infants with type 1 SMA have difficulty swallowing and sucking. They don’t meet typical milestones like … See more
Spinal muscular atrophy (SMA) is a genetic (inherited) neuromuscular diseasethat causes muscles to become weak and waste away. People with SMA lose a … See more
Approximately 10,000 to 25,000 children and adults are living with SMA in the United States. It’s a rare disease that affects one out of 6,000 to 10,000 children. See more
A person with SMA inherits two copies of a missing or faulty (mutated) survival motor neuron 1 (SMN1) gene. One faulty gene comes from the mother and the other … See more
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WEBA waddling gait due to hip abductor weakness is common. Usually, there is minimal or no facial, bulbar, or respiratory muscle weakness, but fasciculations in limb muscles and calf hypertrophy may be seen. Figure 1.
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WEBSymptoms |. Diagnosis |. Treatment. Spinal muscular atrophies are hereditary disorders in which nerve cells that originate in the spinal cord and brain stem degenerate, causing …
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WEBThe primary symptom of chromosome 5-related (SMN-related) SMA is weakness of the voluntary muscles. The muscles most affected are those closest to the center of the body, such as those of the shoulders, hips, …
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WEBSpinal muscular atrophy is a genetic disorder characterized by weakness and wasting ( atrophy) in muscles used for movement (skeletal muscles). It is caused by a loss of specialized nerve cells, called motor neurons that …
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WEBReviewed/Revised Apr 2022 | Modified Sep 2022. VIEW PROFESSIONAL VERSION. Symptoms. Diagnosis. Treatment. Spinal muscular atrophies are hereditary disorders in …
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