What is spinal muscular atrophy and what is its tratment

1. What is spinal muscular atrophy and what is its tratment? Most spinal muscular atrophies are caused by a problem in a gene called SMN1. The motor neurons decompose and cannot send messages to the muscles. In this condition it is must to get in touch with Spine Doctor Nyc. If a child only receives an altered copy of the SMN1 gene from one of their parents, it most likely does not show any signs of spinal muscular atrophy, but it could be passed on to their children. What are the signs and symptoms of spinal muscular atrophy? Some babies are born flaccid or lax (with a great lack of muscle tone) and do not learn to turn around when they are lying down or to sit at the expected ages. An older child may fall more often than children their age or have trouble lifting things. Children with spinal muscular atrophy may develop scoliosis (curved spine) if the muscles in their back are weak. What are the types of spinal muscular atrophy? 1. Werdnig-Hoffmann disease. It begins to affect the infant from the moment of birth or until 6 months of age, but most babies show signs of the disease when they are about 3 months old. Type I : also known as spinal muscular atrophy of onset in lactation or 2. Type II: begins to affect children between 6 and 18 months of age. 3. muscular atrophy, begins to affect the child as early as 18 months or as late as adolescence. Children can walk without help, but they have weakness in arms and legs and fall often. It is the mildest form of spinal muscular atrophy that affects the child population. Type III: also known as Kugelberg-Welander disease or juvenile spinal

2. 4. atrophy type IV do not know that they suffer from it until years after their symptoms begin. Type IV: Since their evolution is very slow, many people with spinal muscular How is spinal muscular atrophy diagnosed? When a Lower Back Pain Treatment Doctor thinks that a child may suffer spinal muscular atrophy, he may ask: • Genetic tests: this is the most frequent way to diagnose spinal muscular atrophy. • A muscle biopsy is when a Chronic Back Pain Doctor removes a small sample of muscle tissue to be analyzed under a microscope. How is spinal muscular atrophy treated? Although spinal muscular atrophy cannot be cured, the following treatments at Chronic Pain Treatment Center can help children who have it. • Nusinersen is a new Lower Back Pain Treatment that was approved in 2016. This medication increases the amount of proteins the body needs due to the alteration in the SMN1 gene. Four doses are administered over 2 months and then, after concluding this guideline, every 4 months. Studies have shown significant improvements in breathing, motor function and survival. •Chronic Pain Treatment that help children cough and clear mucus, which also helps prevent infections • Adequate nutrition Sometimes a tube has to be inserted through the nose that ends in the stomach (called a nasogastric tube) or directly into the stomach (called a gastrostomy tube) to help patients eat.