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SMA (Spinal Muscular Atrophy): What It Is, Symptoms Types SMA is a genetic condition that causes muscle weakness and atrophy due to nerve cell loss in the spinal cord Learn about the five subtypes of SMA, their symptoms, causes and how they affect life expectancy
Spinal Muscular Atrophy | National Institute of Neurological Disorders . . . Spinal muscular atrophy (SMA) is a group of hereditary diseases that affect motor neurons and cause muscle weakness Learn about the five types of SMA caused by SMN1 gene problems, how they are diagnosed and treated, and the latest updates on SMA research
Spinal muscular atrophy - Wikipedia Spinal muscular atrophy (SMA) is a rare genetic disorder that causes progressive muscle weakness and wasting It is caused by a mutation in the SMN1 gene and classified into different types based on age of onset and severity
Welcome to SMA Solar Technology! | SMA America SMA is a global leader in inverters, photovoltaic and solar technology for residential, commercial and large-scale applications Learn about their innovative products, services and vision for 100 percent renewable energy
Spinal Muscular Atrophy (SMA) - Johns Hopkins Medicine Learn about SMA, a genetic disorder that affects motor neurons and causes muscle weakness and atrophy Find out the types, causes, symptoms, diagnosis and treatment options for SMA, including adult SMA
SMA Solar Technology AG - Inverter Photovoltaics Solutions | SMA Solar SMA is a global leader in solar inverters and photovoltaics solutions for homes, businesses and large scale projects Learn how SMA can help you generate, store and use renewable energy with independence and sustainability
Spinal Muscular Atrophy (SMA): Types, Symptoms, Causes - Verywell Health SMA is a genetic disease that causes muscle weakness and nerve cell loss in the spinal cord and brain stem Learn about the different types of SMA, how they are diagnosed and treated, and how to cope with the condition
Causes Inheritance - Spinal Muscular Atrophy (SMA) - Diseases . . . SMA is a motor neuron disease caused by mutations in the SMN1 gene on chromosome 5 It can also be caused by mutations in the UBE1 or DYNC1H1 genes Learn about the inheritance patterns, genetic testing and newborn screening for SMA