Spinal muscular atrophy (SMA): Types and Genetics

Spinal muscular atrophy (SMA) is a rare autosomal recessive neuromuscular disorder characterized by the loss of lower motor neurons (anterior horn cells) in the spinal cord and brainstem nuclei, resulting in progressive muscle weakening and atrophy. The severity and age at onset differ considerably. SMA was initially documented in the …

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Common Genetic Disorders

Genetic conditions are disorders caused by mutations in one or more genes or by abnormalities in chromosomes. In contrast, congenital disorders are not always genetic in origin. They may result from complications during embryonic or fetal development or from issues that occur during the birth process. An example of a …

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