Ame tipo 2, sma tipo 2, atrofia muscular espinal cronica, atrofia muscular espinal. Media in category spinal muscular atrophy the following 8 files are in this category, out of 8 total. Pdf spinal muscular atrophy sma is a genetic disease caused by autosomic recessive trait it affects the anterior motoneurons and causes. Pdf analisis genetico molecular en atrofia muscular espinal. Sma is characterized by the progressive degeneration of the lower motor neurons, leading to muscle weakness and, in the most common. Spinal muscular atrophy sma is an autosomal recessive disease caused by deletions or, less often, point mutations in the smn1 gene, leading to a reduction in the amount of survival motor neuron smn protein. Spinal muscular atrophy power point linkedin slideshare. Childhood spinal muscular atrophy is an autosomal recessive neuromuscular disease characterized by degeneration of the anterior horn cells of the spinal cord. Just recently i emailed my friend and said funny well, not really how many psychologists, doctors, dieticians, support groups, hospitals, and even a hypnotist, i went to over the years that couldnt help me and all it took in the end was a simple site like this, and a supportive partner. Atrofia muscular espinal national institutes of health. Files are available under licenses specified on their description page.
Atrofia muscular espinal ame tratamientos celulas madre. Vorvick, md, clinical associate professor, department of family medicine, uw medicine, school of. Fundacion atrofia muscular espinal mexico cur ame genetic. If you have problems viewing pdf files, download the latest version of adobe reader. Atrofia muscular espinal genetic and rare diseases. Spinal muscular atrophy sma is an autosomal recessive disorder. Ou seja, nao ocorre uma distribuicao homogenea da fraqueza e atrofia muscular. Atrofia muscular espinal spanish medlink neurology. Caso clinico ame tipo i by gonzalo ponce figueroa on prezi. Atrofia muscular espinal tipo 1 genetic and rare diseases. Spinal muscular atrophy sma is an autosomal recessive disorder affecting the anterior horn cells of the spinal cord.
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