What is duchenne muscular dystrophy

September 14, 2021

Duchenne Muscular Dystrophy

Duchenne muscular dystrophy, or DMD, is a genetic disorder that causes muscle weakness and degeneration. This disorder affects mainly boys and sometimes girls, but does not affect the fetus if it is carried by a carrier. A study was conducted to determine how many children have been diagnosed with DMD since the age of 3 in 2003. This study showed that out of 1,719,000 children who were diagnosed with DMD from 2003-2017, only 153 were female. Duchenne Muscular Dystrophy is a genetic disorder that affects boys and typically leads to death in the preteen age range. One of the quickest ways to help them would be through gene therapy. There are many other treatments available to the population, but the DMD patients are choosing gene therapy over these other treatments because it will not only cure their muscle problems but also reduce or completely stop the need for diuretics, oxygen concentrators, and injection therapies. The muscular dystrophies are a group of genetic neuromuscular diseases that cause progressive muscle weakness and wasting. With the understanding that Duchenne Muscular Dystrophy is one of the most common forms, this article provides information about how it spreads, what it means for sufferers, and how to manage the disease.

What is Duchenne Muscular Dystrophy?

Duchenne muscular dystrophy is a genetic disorder that causes progressive muscle weakness in boys starting with their lower body. It is the most common inherited neuromuscular disease with about 1 in 3,500 males being diagnosed with it before age 5. Duchenne Muscular Dystrophy is a type of muscular dystrophy that starts in the teen years and is terminal. Duchenne Muscular Dystrophy is a genetic muscle-wasting disorder that affects boys and young men all around the world. It progresses until eventually, the muscles of the body are so weak that they cannot support standing up without support. Duchenne muscular dystrophy (DMD) is a genetic muscle disease that affects both boys and girls. DMD usually appears between the ages of 3 and 5, but has been diagnosed as early as 1 year old. When DMD develops, muscles weaken over time. The muscles don’t work anymore which makes everyday tasks difficult.

Types of Duchenne

Duchenne Muscular Dystrophy is a genetic disorder, which can result in muscle weakness and loss. The three types of Duchenne are: X-linked, Autosomal Dominant and Recessive. Duchenne Muscular Dystrophy is a progressive, genetic disorder that causes muscle weakness and loss. The different types of Duchenne can be broken down into three main categories: Becker’s Type, Louisiana Type, and DMD – Diagnosed Later. Duchenne muscular dystrophy is a disorder that affects boys and young men. It is caused by the absence of dystrophin, which is one of the proteins in muscle cells. Dystrophin helps to provide structure and strength to musculoskeletal tissue. Other symptoms include muscle weakness, progressive loss of muscle function, cardiac problems, and growth delays. Duchenne Muscular Dystrophy (DMD) is a disease that affects boys and men. It has no known cure and can cause muscle weakness, muscle wasting, and eventual death.

Symptoms of Duchenne

Duchenne muscular dystrophy is a genetically inherited condition that causes muscles to weaken and waste away, leading to disability and premature death. The symptoms of Duchenne muscular dystrophy are varied, but typically show in the form of limited or absent muscle function. Symptoms are caused by loss of dystrophin, the protein that allows muscle cells to contract. The muscle cells die off, causing the muscles to weaken. This starts with the lower limbs and progresses to the trunk, head, neck, and finally to breathing muscles. Symptoms of Duchenne Muscular Dystrophy start appearing when a child is about 3 years old. Symptoms may include trouble walking, leaning, or using hands and muscles. The disease impacts a child’s ability to breathe, speak, eat, and swallow leading to a short lifespan. The symptoms of Duchenne depend on the age of the patient. When a person is born with Duchenne, their muscles will not develop normally. One of the most common symptoms is difficulty walking because the muscles don’t work together correctly.

Treatments for Duchenne

Duchenne Muscular Dystrophy (DMD) is a recessive disorder that affects boys and men, but symptoms become more prevalent in early childhood. Symptoms include difficulty walking and using their legs, muscle weakness, irregular heart rate, and other symptoms that can lead to breathing issues or death. Treatment for DMD includes exercise and medications. Duchenne is a devastating muscle-wasting disease that is the most prevalent in males, with just over 1 in 5,000 boys being diagnosed with this disease. It is caused when the dystrophin gene is not passed down from mother to son. While there are no cures for Duchenne at present, there are treatments being developed in laboratories around the world to try and slow down or stop progression of the disease. Duchenne Muscular Dystrophy is a fatal, genetic disorder that affects boys and young men. Men with Duchenne generally lose their ability to walk by the age of 12, with their strength and muscle mass decreasing as they continue to age. There are currently no treatments or cures for this condition, with only a few managing to live into their teenage years. The first treatment for Duchenne muscular dystrophy was the use of cortisone, which helped to improve muscle function. Other treatments can include supplements that help rebuild muscle, stem cells that promote growth, and various other types of therapy.

Conclusion

Duchenne Muscular Dystrophy is a degenerative neuromuscular disease that causes progressive muscle weakness and wasting, which leads to death. This disease affects boys because it is caused by an X-linked gene on the short arm of their fourth chromosome. It is really important to know the signs of Duchenne muscular dystrophy early on. This way, people can start looking for a cure as soon as they can. Duchenne’s Muscular Dystrophy is a genetic, degenerative muscle disorder that is most notably characterized by the loss of dystrophin protein from the cells in the developed muscles. This protein plays a crucial role in keeping muscles strong and healthy. Duchenne’s affects mainly boys, but girls who carry this gene are also at risk. Duchenne Muscular Dystrophy – a genetic disorder that causes muscle degeneration and weakness – is the most common form of muscular dystrophy in young boys. DMD affects both boys and girls, but the symptoms are far more pronounced in males.

 

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