WHAT Actually Has Been the Stem Cell Therapy for Muscular Dystrophy IN INDIA?

Muscular Dystrophy Stem Cell Therapy India
Muscular Dystrophy Stem Cell Therapy India

A collection of inherited conditions that lead to a gradual decrease of muscle mass and strength over time.

Degeneration of muscles is caused by faulty genes (mutations) in the conditions known as Muscular Dystrophy Stem Cell Therapy India. The majority of cases start in infancy.

Muscles that have been damaged gradually lose their strength. The majority of persons who have the illness will ultimately need the use of a wheelchair. In addition to these symptoms, you may have difficulty breathing or swallowing.

Maintaining function by medication, therapy, breathing devices, or surgery may be possible, although this often results in a shorter life expectancy.


What Are The Causes In Behind the Development Of Muscular Dystrophy?

Muscular dystrophy is brought on by a collection of conditions that are present at birth and are most likely the result of a defect in a single gene.

These conditions interfere with the integrity of the muscle. The faulty coding of the dystrophin gene, which supplies the protein code that is necessary for the creation of muscle tissue, is the root cause of muscular dystrophy (MD).

Weakness in the muscles is often brought on by dysfunctional cells in the muscular tissue, which prevents the muscles from being able to perform their normal functions.

In addition to this, this causes an increase in the number of weak places in the muscles as well as a disturbance in the muscles themselves. The following are some of the factors that might lead to muscular dystrophy.


The Genetic Disorder Known As Muscular Dystrophy Can Be Categorized In One of These Three Ways:

  • This inheritance takes place when both parents pass a defective gene and a normal gene respectively to their child. Due to this new inheritance, both sets of parents have the potential to pass on the faulty gene to their offspring. It indicates that when both parents must be carriers of the mutated gene but must not show any symptoms of the disorder themselves.
  • Their health is only marginally damaged, yet they have one altered gene (referred to as a recessive gene) and one gene that is untouched by the illness (referred to as a dominant gene). Two carriers have a one in three probability of having an unaffected kid who is also a carrier, a one in two possibility of catching an unaffected child who was a carrier, and a one in three chance of having an afflicted child who has two recessive genes that have been modified.


Children Suffering From Duchenne Or Becker Muscular Dystrophy Could:

  • Having difficulty ascending and descending stairs
  • Be clumsy
  • Prone to trips and falls
  • Toe walking
  • Have leg pain
  • weak arm, leg, or face muscles
  • Have healthy and big calves

Both Duchenne (pronounced dew-SHEN) and Becker muscular dystrophies are characterized by progressively worsening symptoms.

This indicates that they become more problematic with time. Children who have muscular dystrophy are at an increased risk of developing scoliosis (also known as a crooked spine), heart difficulties, breathing problems, and difficulty walking.

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