Muscular Dystrophy
PCL Reconstruction Image

Thanks to the development and innovation in research and treatment, degenerative muscular dystrophy now has a treatment with the potential to improve patient condition and facilitate self-dependency. Stem cell therapy for muscular dystrophy treatment in India is proving an effective means of treatment and showing significant positive outcomes.

We, at MedicoExperts understand the dilemma you face in choosing the best and result-oriented treatment for your dear one’s. We empathize with this struggle and therefore, through well-researched and conscious selection, have chosen the best muscular dystrophy treatment approach that will provide positive results and significant outcomes. Our stem experts in India are striving continuously in progressively improving the treatment approaches and combining therapies with stem cell treatment to facilitate better results. Our associated hospitals are fully-furbished with the latest technology and cutting-edge infrastructure and also have a dedicated team of specialists, doctors and medical staff who guarantee round-the-clock care.

Muscular Dystrophy Symptoms

Muscular Dystrophy cannot be diagnosed early in its progression since some of the kids have the normal pattern of development during first few years of their life. Slowly and gradually they start facing problems such as climbing staircase, walking on their toes, getting up from the sitting position etc. Mostly a child with MD, often develops enlarged calf muscles due to fat replacements.

Some of the important symptoms are:
  • Fatigue & muscle weakness.
  • Mental retardation (possible but does not worsen over time).
  • Difficulty with motor skills (running, hopping, jumping).
  • Difficulty in walking.

Best Muscular Dystrophy Treatment in India

Muscular dystrophy (MD) refers to a group of more than 30 genetic diseases which shows rapid muscle degeneration causing muscle weakness. It generally manifests before the child turns 6 years old, where the body muscles begin to degenerate with time leading to the child feeling weak. The deteriorating progresses rapidly and will eventually cause muscular damage to the heart and respiratory organs. Muscle weakness is the main and basic symptom of muscular dystrophy which leads to difficulty to carry out the daily functional activities. These disorders vary in age of onset, severity, and pattern of affected muscles. All forms of muscular dystrophy grow worse as muscles progressively degenerate and weaken.

With the use of stem cell therapy for muscular dystrophy, the stem cell experts aim to remodel the tissue in the patient, reduce inflammation of muscles and to also prevent the rapid deterioration of cells. However, stem cell therapy in India is a unique mix of proven therapies like Hyperbaric Oxygen Therapy (HBOT), gene therapy, physical therapy, rehabilitation, etc. which are used along with stem cell therapy to customize a treatment plan to yield the best results. The best muscular dystrophy treatment in India is made possible due to the technological advancements and effective treatment procedures employed by the best stem cell experts in India.

Reasons to Choose India for Muscular Dystrophy Treatment

The treatment for muscular dystrophy through means of stem cell therapy and other therapies is a highly advanced and result-oriented treatment module that is yielding significant results. All the best doctors in India have their own unique and specific treatment mode based on the challenges faced by the patient. Some of the key reasons to choose India are:

Combination of advanced therapies with stem cell therapy for result-oriented outcomes

Fully-furbished medical facilities with cutting-edge technology and dedicated team of medical staff, doctors and specialists

International standard of treatment, accommodation and care

Cost of Muscular Dystrophy Treatment in India

India is one of the most cost-effective and result-oriented destination to choose to undergo stem cell therapy. With the availability of state-of-the-art hospitals, best stem cell experts and excellent infrastructure which is at par with international standards, you also get affordability and trustworthiness. The stem cell therapy for muscular dystrophy treatment in India is based on the patient’s requirement and medical condition.
The cost of stem cell therapy in India starts from USD 2000 per cycle, depending on the patient’s current condition, treating doctor and suggested treatment protocol. A stay of 12-15 days in the country is requirement for the entire treatment, and in some cases the stay maybe extended to 45 days as well. Depending on the protocol of the chosen specialist stem cell therapy will be clubbed with latest and advance therapies like ozone therapy HBOT, stimulations and many more for better results. The cost of Hyperbaric Oxygen Therapy (HBOT) ranges between 50 – 90 USD per session. Each session lasts for about 60-90 minutes for 25-30 days, every day.

Muscular Dystrophy

Muscular dystrophy (MD) is a neuromuscular disorder that constantly damages the healthy muscles making them weak and wasted. The disease is a form of congenital abnormality due to wrong expression of faulty gene. Muscles and membranes need many different proteins to be strong and function properly and these proteins are supplied to our body from the food we eat but some of them are synthesized by our own body such as Dystrophin.
This information regarding the production as well as the amount of protein is being passed on, by our own genetic makeup. Due to gene mutation wrong information is passed from one generation to another generation due to which these important proteins are not produced or produced in very low quantities. Without these proteins, muscles lose their structural and functional integrity slowly which may affect the overall normal functioning of the body.

Conventional Treatments for Muscular Dystrophy

Prior to the use and development of stem cell therapy, the conventional treatment approaches for muscular dystrophy were aimed at provide mobility and aid in strengthening the muscles of the heart and lungs.
The previously available treatment options included physical therapy, occupational therapy, medication and surgery. Depending on the extent of difficulty faced by the patient, treatment plans are made to help manage trouble in swallowing, breathing, walking and hand movements and also to slow the deteriorating of muscle tissues.

• Medication

The doctor may prescribe certain medications to help with the condition. Through medication the doctor aims to delay the progression of the condition and also strengthen the muscles. In cases where there is probable heart damage, heart medication is also recommended.

• Exercises

Low-impact work-outs like stretching, walking, etc. will help maintain muscle movement and improve overall health. Under the careful supervision and guidance of a doctor, the patient can also do some exercises to retain range-of-motion of the muscles which otherwise is affected by muscular dystrophy. These exercises will help in keeping the muscles and joints flexible.

• Therapies to improve length and quality of life

Several types of therapy and assistive devices can improve the quality and sometimes the length of life in people who have muscular dystrophy. Braces and mobility aid will help provide support to the weak muscles and also provide self-dependency. The braces will also help in keeping the muscles and tendons flexible and stretched, thereby reducing contracture progression.

• Surgery

Surgery may be required to correct the spinal curvature or contractures which could lead to trouble in breathing. In cases where the heart function maybe affected, surgery to implant a pacemaker or other cardiac devices is done.

Advanced Treatment Options for Muscular Dystrophy

1. Stem cell therapy

Recent research has proven that stem cells have the potential to regenerate and repair the damaged muscle cells. Stem cell therapy is one of the effective treatments for MD as it provides cells that can both deliver functional muscle proteins and replenish the stem pool. Transplanted cells have myogenic potential i.e. the cells can divide into a mature myocyte and then can repair and regenerate muscle fibres. Pre-clinical evidence ensures that stem cell therapy can restore dystrophin protein which leads to formation of muscle fibres that are resistant to easy damage and degeneration.
Stem cells are known to have a tangible approach in the treatment for MD. These cells by his natural property can regenerate affected muscles by inducing myogenesis and provide a decent symptomatic relief. As the expected deterioration of patients of MD is about 20% every year, an improvement in percentage of deterioration after Stem Cell therapy is proven and observed by most doctors. Stem cell therapy can halt the growth of the disease which can prevent further complications of the disorder.

2. HBOT therapy

Stem cell therapy together with advanced hyperbaric oxygen therapy (HBOT) technology has turned into the highest possible blend of benefited muscular dystrophy treatment. HBOT mobilizes human bone marrow stem cells that can assist in muscle cell regeneration. Based on these results, it is recommended that HBOT in patients with MD improves symptoms and facilitates the functions of stem cells.

3. Ozone therapy

It is used as an alternative therapy to improve the intake and oxygen use of the body and to activate the immune system. Ozone therapy is one of the most potent ways to flood your body with additional oxygen drastically and quickly. Not only does ozone itself have incredible healing capabilities but this fact has also been well documented for centuries. Combined with stem cell therapy, ozone therapy yields successful outcomes

Successful Treatment of Muscular Dystrophy in India

Successful stem cell treatment for muscular dystrophy aims to restore and slow down muscle wasting which occurs in muscular dystrophy. Our research and years of successful treatment of muscular dystrophy in India has resulted in patients showing significant improvement. Over 90% of patients with muscular dystrophy have shown improvement in muscle strength, mobility, improved hand function, increase in stamina, and also improved balance and limb strength. Our patients have exhibited notable improvements in multiple ways that demonstrate the advantages of cell therapy in India for muscular dystrophy. The strength and tone of the muscles improves after stem cell therapy as a result of new muscle fibres which consequently helps reduce symptoms and improve condition.

Best Doctor for Muscular Dystrophy in India

The best doctors for muscular dystrophy in India employ the use of advanced therapies like stem cell therapy along with HBOT and other therapies to provide beneficial results. Here is a list of top specialist and doctors in India for muscular dystrophy treatment:

Best Hospitals for Muscular Dystrophy in India

The best hospitals in India are fully-furbished with the latest technologies to successfully treat patients with muscular dystrophy. Here is a list of our best hospitals for muscular dystrophy treatment in India:

Why choose MedicoExperts?

At MedicoExperts, we understand the significance of your health, well-being and importance of leading an independent life. Our aim is to provide you the best experience for Stem Cell treatment in India at our top associate hospitals in India. Your Believe and trust of on us is our responsibility. For your privacy and protection, we maintain a strict non- disclosure policy. We understand that while you choose to travel abroad for your Stem Cell Treatment, you would surely look for positive results, comfort and guaranteed result.

We would also provide you end to end assistance for your medical trip to India and shall provide complete solution for your Stem Cell Treatment – right from assisting you with the visa, hotel arrangements, airport pick up and drop, inland transfers, money exchange or sight-seeing and all other concierge services. We thus assure you hassle-free arrangements for evaluations, treatment, stay and travel in India.

For a faster and guarded means of communication, you can always get in touch with us by sharing your medical history and diagnostic reports to

Frequently Asked Questions and patient concerns:

1. What is muscular dystrophy?

Muscular dystrophy (MD) is an umbrella term for more than 30 genetic diseases that cause progressive weakness and degeneration of the muscles used in movement.

DMD is suspected when children present with walking difficulties usually around the age of 2 or 3 years.

Depending upon impaired gene, site where the gene is located, and the progression of symptoms muscular dystrophies are divided into various types. Major forms of Muscular Dystrophy:

  • Duchenne Muscular Dystrophy: This is the most common form of muscular dystrophy which affects the boys. The symptoms are usually observed during 2-3 years of age. The child becomes wheel chair bound at the age of 12 years and dies of respiratory failure by his early 20’s. As this involves the weakness of major involuntary muscles such as heart, lungs, etc.
  • Emery Dreifuss Muscular Dystrophy: This is a very rare form of MD, typically observed in late childhood to early teens. Symptoms are the same such as wasting of muscles, weakness, join deformities with slow progression. In severe cases, sudden death may occur due to cardiac arrest.
  • Limb-girdle Muscular Dystrophy: This is a type of muscular dystrophy, that affects both boys and girls, usually occurring in late childhood to middle age. The symptoms include muscle atrophy in shoulders, upper arms, around the thighs and the hips
  • Myotonic Muscular Dystrophy: This is a type of Muscular Dystrophy, in which muscle relaxation can cause a problem occurring especially in teens. Some other problems such as muscle weakness, wasting, cataracts and heart problems are commonly observed.
  • Facioscapulohumeral Muscular Dystrophy: This type of Muscular Dystrophy occurs in both men and women but predominant in men. The symptoms may include sleeping with their eyes slightly open, an inability to squeeze their eyes tightly and an inability to bring their lips together.

Although all muscular dystrophy is genetic, about one third of the families of DMD patients have no prior history of the disease. This is because DMD may occur as a result of a spontaneous genetic mutation.
Genetic counselors at Stony Brook Children’s Hospital can offer detailed information about genetic testing and inheritability.

Babies, teens or adults can face the muscular problems at any phase of their development as this is caused due to muscular weakness. About 1 in every 3,500 boys worldwide is born with the most common form of the disease, Duchenne Muscular Dystrophy (DMD)

Due to genetic defects the proteins that are formed by the genes are either absent or less functional. The group of proteins that are affected in different muscular dystrophies are called Dystrophin Sarcoglycan Complex (DGC). DGC is important to maintain the structure of the cell wall of the muscle cell called Myocyte.
Muscle degeneration occurs due to bad structure of the cell wall of myocyte (muscle cell) even with day-to-day muscle activity. This uncontrolled degeneration leads to rapid muscle death and weakness which ultimately leads to muscular dystrophy. Uncontrolled muscle death is the primary cause of muscle weakness. Due to continuous muscle degeneration, there is chronic inflammation which damages muscles even more. Along with muscles of the body, the muscles of cell walls are also affected which affects the blood supply to the muscles causing more damage. As DCG is also present in various non-muscular tissue like nerves, kidneys, spleen and Schwann cells so muscular dystrophies may also show some neurological symptoms.

Some forms of MD appear in infancy or childhood, while others may not appear until middle age or later. Each of the dystrophies causes progressive skeletal muscle deterioration and weakness, but severity and life expectancy vary.

DMD is caused by a mutation on the X, or male sex chromosome, so it mostly affects boys. However, girls and women who carry the defective gene may show some milder symptoms.

DMD is a genetic disorder. There are no tests to detect DMD in a child before birth. However, genetic counseling helps in the identification of at-risk families.

Talk to us, we are here to help

Make an appointment