The muscular dystrophies are a cluster of hereditary illnesses designated by progressive muscle degeneration and feebleness. In some types of this disease, the heart and other organs are also affected.
Types of muscular dystrophy
There are 9 kinds of muscular dystrophy:
Symptoms and consequences
In dystrophy, a specific portion of the body deteriorates or withers. In muscular dystrophy, the weakness is present in the muscles. A hereditary genetic slipup stops the body from making a protein that helps build muscles and keep them sturdy. Kids who are born with muscular dystrophy generally develop normally for the first few years of life. They might unexpectedly reveal signs of clumsiness. Over the years, kids with muscular dystrophy can become feebler and weaker, losing the ability to sit, walk and lift things. The ailment can also affect muscles in the heart and lungs, serious heart and respiratory complications can also befall. There are diverse kinds of muscular dystrophy. Muscle weakness is a characteristic of every type. But the symptoms can vary and begin at diverse ages. Some muscular dystrophies are mild; others are extreme and can cause grander muscle loss.
Recognizing the symptoms timely on can help the parents begin treatment as rapidly as possible. Early diagnosis is also imperative so the muscular dystrophy treatment in India can begin promptly. This disease can be efficaciously cured by stem cell therapy.
At StemCellCareIndia, we offer a comprehensive range of stem cell solutions in India for the treatment of muscular dystrophy.