What Spinal Muscular Atrophy?
It’s Roya, a seemingly ordinary 15-year-old girl until she begins to struggle with her everyday tasks. Roya was diagnosed with Spinal Muscular Atrophy (SMA) at the age of two and has had difficulty walking since then.
The blog post What Spinal Muscular Atrophy? shares the story of a young boy with Spinal Muscular Atrophy (SMA) and the steps that his family took to raise awareness as well as money for research. The main goal of the article is to share these efforts and inspire people to take similar actions in their communities.
What Spinal Muscular Atrophy? I can’t thank you enough for promoting my story. I am looking forward to reading your article and hearing about what else is happening in the world.
What Spinal Muscular Atrophy? When you think of “disabilities” to your child, what do you immediately think of? Do you see them in a wheelchair or can they not walk? What about if they cannot talk or use their arms like other children their age? For CJ and her family, she has something called Spinal Muscular Atrophy (SMA). This is where the lower part of the body starts to weaken and the nerves don’t work as well.
What Spinal Muscular Atrophy? Patients with Spinal Muscular Atrophy (SMA) are now living longer than ever before. Find out how the disease is managed and what treatments are available in this article.
What Spinal Muscular Atrophy? Meet little Zoey, a 4-year-old girl with Spinal Muscular Atrophy. After being diagnosed at birth, she quickly became unable to do the things most children take for granted. She couldn’t walk, couldn’t sit up on her own, and wasn’t able to talk. Doctors estimated that she had only 3 years left to live.
In this article,What Spinal Muscular Atrophy? we will explore the life of a person with Spinal Muscular Atrophy. We will learn about the difficulties that they have to go through in order to move from one place to another. Learn how they live their lives and what struggles they face on a day-to-day basis.
Spinal Muscular atrophy Detailed Explaination
Spinal Muscular atrophy is a genetic disorder in which the motor neurons of the spinal cord are progressively lost, leading to increasing muscle weakness. The cause of SMARD is currently unknown, but it has been linked to an incorrect gene that prevents the body’s cells from breaking down certain proteins.
Spinal muscular atrophy (SMA) is a genetic disorder that primarily affects the motor neurons in the spinal cord. SMA is characterized by progressive muscle weakness of varying degrees and decreased or absent deep tendon reflexes. The disease progresses from birth to adulthood and typically results in death of the individual within 2 to 9 years of diagnosis.
Spinal muscular atrophy is a disorder of the nervous system that causes progressive muscle weakness and loss of motor control. The symptoms vary from one child to the next, but typically include difficulties in moving, such as crawling or walking.
Spinal muscular atrophy is a rare genetic disease characterized by progressive muscle degeneration and weakness. It typically affects one in 10,000 children worldwide, but can also impact adults. The disorder is caused by the loss of the SMN1 gene from both copies of chromosome 5, which leads to decreased amounts of survival motor neuron (SMN) proteins.
Spinal Muscular atrophy is a disease that is caused by the deletion or mutation of the SMA gene. The SMA gene codes for the production of a protein called survival motor neuron (SMN) protein. Lack of the SMN protein causes Spinal Muscular atrophy because it causes problems with motor neurons. The SMN protein helps these neurons function properly which keeps the muscles strong and functional. Muscle weakness is one of the first signs of Spinal Muscular atrophy.
Spinal muscular atrophy is a type of motor neuron disease. The condition is caused when the spinal cord is damaged from either a genetic mutation or an environmental factor. As a result, the nerve cells in the muscles of the body do not work properly and this leads to muscle wasting and eventually death.
Symptoms of Spinal Muscular Atrophy
Spinal Muscular Atrophy or SMA is an incurable disease that weakens the muscles. Some of the most common Symptoms of Spinal Muscular Atrophy are weakness in the hands and feet, difficulty sitting up, poor feeding, and delayed milestones. Children will also have difficulties with breathing because of weak chest muscles.
Spinal muscular atrophy is a genetic disorder. It’s one of the most common inherited diseases in children. It affects the voluntary muscles, which are used for everyday activity like walking and speaking. The Symptoms of Spinal Muscular Atrophy gradually get worse over time.
Symptoms of Spinal Muscular Atrophy are, in general, progressive. However, they are not always present from birth. They include muscle weakness in the trunk, arms and legs. Other symptoms may include difficulty swallowing, impaired breathing and speech difficulties.
The most common symptoms of spinal muscular atrophy are the inability to walk, difficulty sitting without support, and shaking or trembling in the arms. This can also happen with difficulty swallowing, slurred speech, and difficulty breathing.
The signs of SMA can vary by what type of SMA you have. The most common signs are muscle atrophy, loss of head control, and the development of scoliosis. There are four types that affect different parts of the body. Type I affects the anterior horn cells in the spinal cord while type II affects the anterior horns and lower motor neurons. Type III is when all three affected portions are present while type IV affects only lower motor neurons in the lumbar spine.
Spinal muscular atrophy is an inherited disease that leads to progressive muscle loss in the arms, legs, head, and trunk. It’s most often diagnosed in toddlers or young children between the ages of three months and five years old.
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