#Elyoum elsabea full#

It also allows them to know the probability of their children having muscular dystrophy and their ability toįollow up and perform the necessary tests at a very early stage, where genetic testing plays a very important Whether their children are allowed to marry their cousins, as this is sometimes common in some provinces inĮgypt. Is transmitted by heredity and this allows us to know whether they are allowed to marry their cousins or However, what they should consider and take intoĬonsideration is genetic counseling when they decide to have children so that they can discover how the disease Which means they can get married and have children.

People who suffer from muscular atrophy, with the suitable follow-ups, patients now can have a normal life, Adults with muscular atrophy can only perform certain jobs that do not require much movement and they need someone to take care of them at a certain stage. This often means that a parent has to give up his normal life to afford extra care for this child. For children with muscular atrophy, parents should send them to private schools and must be given intensive and continuous care. Muscular dystrophy patients and their families suffer from a very difficult life. How does the life of people with muscular dystrophy look like? The Department of Health must approve all treatments, even if approved by the FDA, and the Ministry conducts very rigorous tests and researches on each treatment prior approval, in other words that means that once it is approved it will be 100% guaranteed. Shown that this might cause severe complications. Therefore, from my own point of view, I can not say that stem cells therapy is successful. There have been researches about stem cells therapies, some claim it is used to treat muscular atrophy however, there are no enough research work and experiments to prove the success of stem cells therapies. They have acquired muscular strength as well as improved respiratory muscles, which means they no longer need respiratory support. Many patients worldwide are being treated for the time being.

The Food and Drug Administration (FDA) has now approved treatments for some types of muscular dystrophy, and more treatments are still in its third testing phase in the Food and Drug Administration, indicating that it will soon be approved.

#Elyoum elsabea full#

It is important to note that muscular dystrophy is a treatable but incurable disease, and patients can still live a full life with the right treatment. There is another muscular dystrophy type named 'Duchenne', which begins to appear when the child is able to run, jump and climb stairs, but he is unable to do so, as a result of muscle weakness. Often due to the reason for the presence of a large defect in one of the proteins responsible for working on strengthening the genes muscles, as this imbalance appears at an early age or at a later stage of life depending on the percentage of the lack of this protein and its function in muscle building process.Ī 'spinal muscular atrophy' are three types a type of spinal muscular atrophy begins in the new born babies, where the neck support is very weak barely be able to lift his head up or sit and it often causes problems in the respiratory system and then the baby needs respiratory support to be able to breath. Muscular dystrophy is a group of inherited diseases that affect the muscles gradually, and there are more than 50 kinds, according to the protein or enzyme damaged by the body.