Unfortunately, if you or someone suffers with muscular dystrophy (or MD) then the first worst thing that may make you surprise is that no proper cure or treatment against it has come out so far. Even then, it is worthwhile for you to be on the ball about the causes, symptoms and provisional treatments. Well, Muscular dystrophy is a genetic disease that passes down from generation to generation and causing the different muscles of the patient to weaken and deteriorating with passage of time. The MD subsists in several different forms, which can tell upon different muscles of the body and therefore pose respective harmful results.
As Muscular Dystrophy is genetic in nature, the mother is presumably the fundamental carrier, and the disease specifically transfers to their male children. However, in Facioscapulohumeral MD, a specific type, both males and females are affected uniformly.
As MD specifically attacks the male infants, the females usually have a lesser chance to become the victim of this genetic disease. Luckily, through the innovative machines, it is possible to diagnose the embryo infected by the muscle dystrophy gene in the course of pregnancy. If someone in their lineage has been witnessing the recur of MD then it is very important to have a diagnosing test and the truth will be out.
The symptoms of Muscular dystrophy usually vary in accordance of the intensity it poses on the patient’s body. Facioscapulohumeral MD basically tells upon the patient’s upper body part and the face.
And there are also other complications like Droopy eyelids, problem in hearing, difficulty in pronouncing words and unattractive facial expression altogether constitute Facioscapulohumeral MD’s syndromes. Alternatively, Becker’s MD affects the lower part of the patient’s body including the legs and the pelvis.
Despite there is actually no cure for Facioscapulohumeral MD as well as Becker’s MD, it is possible for one to sustain the life in a regular style but with some or no complications.
Duchenne’s MD is the most dangerous of all and typically causes the patient to be constraint to a wheelchair and prove fatal in certain instances. Contraction in the muscles is seemingly the common thing to observe and certain other complications can also follow in the course of the disease. Most young people suffering with Duchenne’s Muscular dystrophy have been found to give up the ghost by the age of 25.
Despite having no cure for Muscular Dystrophy, the available treatments lay basis on strengthening the muscles and cutting back the intensity of the syndromes.
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