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Gene mutations can not be all turn as the information in the gene has become nonadaptive . Although , the muscular dystrophy can be reversed in some cells through gene therapy , but this therapy is in a very initial stage .
Can Muscular Dystrophy Be Reversed?
Muscular muscular dystrophy is disease which does not have any cure . Further , this disease involves gene mutation thus it can not be completely reversed.1The disease is build up in a patient through two fashion . In innate muscular muscular dystrophy , the disease is inherited form the parents . It is to be note that the heritage of the disease is dissimilar in males and females . It is inherited in X - linked chromosome recessive pattern . The other way through which the disease is developed is acquired . The disease can be gain afterward in the life through spontaneous chromosomal mutation in the gene . The congenital disease has more severe symptoms as compared to get form .
Further , unlike powerful dystrophy mutations occur in unlike stages of life-time . Thus , one form is more dominantly found in childhood while other course is commonly chance in adults . The variation in the genes is very hard to be reversed . Mutation is the cognitive operation of changes in the social structure of the genes and the information which is present in them . Gene therapy is the process through , which newfangled and sizable genes can be comprise in the musculus cell , but this therapy is under visitation . Although the staring circumstance of muscular dystrophy can not be reversed or cured , but the consideration can be make do through integrate approach .
The approach in the management of hefty dystrophy is to slow the patterned advance of the disease so that the life sentence duo of the patient is increased , reduction in the symptoms , improving the quality of life and wee-wee the patient independent . Various drugs are used to slow down the disease progression , and exercise is advised to boil down the symptoms such as muscle clumsiness . Further , various aids such as braces , wheel chairs or walker are used by the patient to ameliorate the quality of life .
Muscular Dystrophy Prognosis
Speed Of Progression Of Disease : If the speed of forward motion of the disease is very high , the patient has short medical prognosis . However , if the procession is slow up by drugs such as steroids or immunosuppressants , the patient has favourable prognosis .
Response Of The Patient Towards Treatment : Although the muscular muscular dystrophy is incurable disease , but various treatment regimen delay the progression of disease and amend the quality of lifespan . Thus , if the patient role positively responds to the treatment , there is a favourable prognosis .
Muscles Affected : Although all the muscles of the body are crucial , but some muscular tissue perform the vital functions . These functions include cardiac mathematical function , respiratory use and brain function . If these muscles are affected by the powerful dystrophy , the patient may get life - threatening ramification and sudden dying may take place . Thus , if the vital muscles are affected , patient have poor prognosis .
Source Of Disease : reference of the disease also affects the prognosis of muscular dystrophy . innate muscular dystrophy shows more hard symptoms as compare to acquired muscular dystrophy . Thus , affected role having congenital shape has poor prospect as compared to acquired conformation , provided other agent are vulgar .
Degree Of Muscle Weakness : Various forms of hefty dystrophy exists . In one form of muscular dystrophy , the gene mutation occurs in such a way that the synthesis of dystrophin is completely absent.2This is a grave variety of the disease and the patient have relatively pathetic medical prognosis . In other form of muscular dystrophy , gene genetic mutation take place in such a way that the dystrophin so form is smaller than the original one . These affected role have favorable prognosis .
Conclusion
brawny dystrophy can not be reversed in the same cell in which chromosomal mutation has occurred . Although the condition can partially be revoke through gene therapy , but this therapy is in very nascent phase .
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