Muscular Dystrophy Treatment Needs Physical and occupational therapies that strengthen and stretch muscles which helps to maintain function and range of motion

 


Muscular dystrophy is a group of disorders characterised by gradual muscular weakness and loss. Mutations in faulty genes cause muscular dystrophy, which prevents the creation of proteins needed to make healthy muscle. Muscular dystrophy comes in a variety of forms. The most frequent variety's symptoms appear in childhood, particularly in boys. Other varieties don't show up till later in life. Muscular dystrophy has no known cure. Medication and therapy, on the other hand, can help manage symptoms and reduce the progression of the condition.

Muscular Dystrophy Treatment are currently available can help control and minimise the severity of symptoms. Treatment research, including some gene-based approaches, is also showing promise in decreasing or even reversing some symptoms of specific forms of MD. The therapies or drugs that may be utilised or prescribed for patients with MD are not covered in detail in this article. Please speak with your healthcare professional if you have any questions about MD treatments. The National Institute of Neurological Disorders and Stroke leads NIH research on MD (NINDS). More detailed information about therapies can be found on the NINDS page on MD.

Muscular dystrophy is a disease that frequently runs in families. A child with a muscular dystrophy parent may inherit a mutant (changed) gene that causes the disease. Although some people carry the defective gene, they do not suffer muscular dystrophy. Healthy individuals (carriers) can transmit the faulty gene on to their children, who may develop the disease.

According to a study published in the Karger Journal in 2014, the global prevalence of muscular dystrophies ranged between 19.8 and 25.1 per 100,000 people per year, with myotonic dystrophy (0.5-18.1 per 100,000), duchenne muscular dystrophy (1.7-4.2), and facioscapulohumeral muscular dystrophy (3.2-4.6 per 100,000) being the most common. The global muscular dystrophy treatment market is driven by the initial research phase of medicines and ongoing clinical studies for the development of innovative products.

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In addition, the United States Food and Drug Administration (FDA) established specific guidance for drug development for muscular dystrophy medications in 2015, which is intended to speed up the development of new drugs for the treatment of the illness. The advent of disease-modifying medicines as a replacement for unmet medical needs of patients who are not susceptible to mutation-specific drugs is predicted to drive the global muscular dystrophy treatment market revenue over the forecast period. However, the rapid prognosis of a problem and poor treatment seeking rate as a result of delayed diagnosis are the key restraints on the worldwide muscular dystrophy treatment market's growth.

Most forms of muscular dystrophy are caused by genetic abnormalities or alterations. Even if neither parent has the illness, one or both parents may convey a defective gene to their child. Muscular dystrophy can occur spontaneously, which means there is no recognised reason. The most common symptom of muscular dystrophy is muscle weakening. The disease affects different muscles and regions of the body depending on the type.

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