Get Familiar With Muscular Dystrophy In Detail

Muscular dystrophy is not a single ailment, it is an amalgamation of ailments affecting muscles and destroying them gradually. These ailments vary from each other in the muscle confronted firstly, development of disease and their pattern of inheritance. The characteristic of the ailment is feebleness of skeletal muscles because of defects in the creation of muscle proteins eventually leading to death of cells and tissues of the muscles. Thus, there is liberal spread of the disease and leads in death of the patient.


Muscle dystrophies are hereditary maladies. The pattern of inheritance varies with the category of dystrophy. The most common type, known as Duchenne muscular dystrophy (DMD), follows an X-linked inheritance. To simply put, the genetic factor that causes dystrophy is existing in the X sex chromosome. Males have only one X chromosome and consequently the presence of transformed X chromosome would cause the ailment. Ladies, alternatively, have two X chromosomes and the modified genes should be present in both to cause the disease. Thus it is said that DMD follows an X linked receding pattern of inheritance. Accordingly, maximum females act as transporters of the disease. This kind of muscle dystrophy cannot be passed on from a father to his son. Since these are hereditary disorders, they run in families. There are exemptions where in the ailment is triggered by a transmutation in the concerned gene.


There are nine ailments which are categorized under muscular dystrophies. These are Duchenne, Becker, limb girdle, myotonic, oculopharyngeal, distal, congenital, facioscapulohumeral and Emery-Dreifuss. These categories vary in their appearances in heart, endocrine system, eye, skin, gastrointestinal, nervous, other organ systems and arrangement of progress there.


The most universally observed symptoms are faintness of muscles that upsurges gradually, recurrent falls because of poor balance and struggle in walking, contractions of muscles, trouble in breathing occurs infrequently, fatigued eyelids, curving of spine, under development of gonads, frontal baldheadedness, cataracts, mental damage, pain of calf muscles supplemented with wobbling gait and restricted movements. Some MDs affect the heart muscles resulting in cardio-myopathy. The symptoms mentioned are usually not spotted until a diagnosis of the condition is made. Also, the symptoms differ with type of MD and age of onset.


If an individual wants to find a sure-fire way to treat this ailment, he or she can confidently resort to stem cell treatment for muscular dystrophy in india that is proved to be highly effective.

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