Stem Cell Care India

What Exactly is Muscular Dystrophy and Its Symptoms?

Muscular dystrophy is a term first devised in the 1890s. It refers to some hereditary ailments which are categorized by progressive deterioration of muscle. There are numerous diverse types of dystrophies, but the most common is Duchenne muscular dystrophy and the symptoms are defined here. This is a progressive muscular ailment characterized by proximal muscle (the muscles closest to the trunk) weakness and worsening. It chiefly affects boys and becomes obvious between the ages of 2 and 6 years. Progress of the infection is speedy. Walking becomes challenging and by puberty a wheelchair is generally essential. The prognosis is poor, demise typically happening during the late teens or initial twenties.

Beginning of muscular dystrophy is normally around 3-4 years of age. The symptoms of muscular dystrophy or its signs might be detected earlier or ignored, contingent on the family past. The muscles which first exhibit signs of feebleness are those around the hips, thighs and shoulder. There might be postponement in walking or failure of the gait to become stable and harmonized. The kid might fall often without obvious reason. Traversing the steps of stairs is often very challenging. Ultimately the gait adopts a typical wobble with the feet placed apart and an overstated lumbar arc. The kid walks on his toes. This permits the line of gravity to fall outside the vertebral column, giving better steadiness. Numerous kids with muscular dystrophy also have intellectual damage, chiefly encompassing memory and verbal abilities and this can be improved with stem cell muscular dystrophy treatment.

  • Love
  • Save
    Add a blog to Bloglovin’
    Enter the full blog address (e.g.
    We're working on your request. This will take just a minute...