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Muscular Dystrophy Treatment

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Muscular Dystrophy

Muscular dystrophy is a group of disorders, characterized by progressive degeneration of skeletal muscles and muscle weakness. There are nine different types of dystrophies and all of them are associated with the faulty gene dystrophin that creates a defect in muscle protein, leading to progressive damage of muscle cells and tissue. Most of these muscular dystrophies are multi-system disorders with manifestations in different systems of the body, such as the cardiovascular system, gastrointestinal system, nervous system, endocrine system, etc. Thus, children with muscular dystrophy typically succumb to paralysis and eventually death in their early twenties due to respiratory failure and cardiac complications. In the majority of the cases, the symptoms are apparent in early childhood by the age of 3-5 years, when the child has difficulty in walking and controlling body movements.

Although, conventional treatment options are limited, recently, due to successful therapeutic benefits of stem cells, proven in pre-clinical analysis; a keen interest has been developed in using stem cells for muscular dystrophies, with the hope that they are effective in regenerating muscular damage.

Stem Cell Therapy for Muscular Dystrophy: Advancells Protocol

At Advancells, we have identified the unlimited potential of stem cells isolated from different Adult Autologous sources of human bodies, including Bone Marrow, Adipose Tissue, etc. With our advanced Technical Support, Scientific Excellence and Competent Quality Management System, we are focused to provide a comprehensive, personalized therapeutic solution that is best suited for individual requirements of people undergoing treatment for Muscular Dystrophy.

 

The Entire Treatment Process at Advancells is divided into 4 steps

 

Treatment Qualification

Source Extraction

Processing of stem cells

Re-infusion

Advancells has come up with unique technologies to offer freshly expanded cells with much better efficiency & viability for all your therapeutic need

Recovery of more than 94% cell count which is up to 20 times more than other dated technologies.

Research oriented company focused on therapeutic applications of Regenerative Medicine.

Delivering technologies for safe and effective regenerative therapies for patients with the highest medical standards.

World-class GMP lab at the forefront of R&D for finding natural, safe and effective therapies for life-threatening diseases & for preventive healthcare, cosmetic treatments and Anti Ageing Therapies.

Must Read Articles on Muscular Dystrophy

Cell Treatment – Effective For Duchenne Muscular Dystrophy (DMD)

Duchenne Muscular Dystrophy (DMD) is a childhood genetic condition that results in muscular disorder, especially in skeletal muscles. Even though the child is born with the genetic condition, symptoms are not visible at birth. Muscle weakness develops gradually and...

Is Stargardt’s disease blurring away your vision?

Our eyes are the window to this world. A blurred vision can be traumatizing emotionally and mentally. This can be attributed to several reasons including damage in retina. The retina is the portion of the eye responsible for sensing light and transmitting the...

Unravelling the Science Behind Muscular Dystrophy

We are all born with a definite pool of stem cells in our muscles known as the “satellite cells” which are present in a dormant form or quiescent state. During childhood, they are activated to form new muscle fibers while in adulthood they are mainly involved in...

Treatment of Muscular Dystrophy with Stem Cells Isolated from Different Sources

With the establishment of various feasibility and safety standards using Stem Cell Therapy on animal models of muscular dystrophies, researchers are trying out several channels to utilize the potential of stem cells for preventing muscle wastage. Mesenchymal Stem Cells, present in various potent niche of the human body, have proven to be very effective in producing working muscle fibers that can eventually replace the damaged ones and restore the lost and/or weakened muscular functions. Different studies have also pinpointed that with the infusion of Mesenchymal Stem Cells, characteristic muscular inflammation associated with MD can be reduced to a great extent, especially due to the release of different chemical messengers. This can further prevent the disease progression and increase the lifespan.

Download the information pack today to understand, everything you need to know about different types of muscular dystrophies; and Advancells Stem Cell Protocol.

Recent Testimonials for Muscular Dystrophy

Over the past couple of years, many clinical studies have been conducted using stem cells isolated from different sources, including but not limited to fetal-derived Allogenic sources, and have demonstrated complete safety, feasibility, and efficacy in reducing muscle wastage and other complications.

With pioneering experiments and outcomes in the preclinical investigations, almost 70-80% of the patients, treated at Advancells using Mesenchymal Stem Cells, have indicated restoration of a considerable proportion of muscle fibers. Although the degree of improvement is quite variable, based on reported claims, we can successfully report positive improvement in areas, such as:

  • Reduced episodes of muscular weakness, twitching, and stiffness
  • Significant improvement in the volume of muscle fibers
  • Improved mobility
  • Improved functional restoration
  • Better cognitive and motor skills

Upload your reports today for a free online consultation

Advancells

A-102, Sector-V Noida-201301, UP, India

Tel: +91-9654321400

Email: info@advancells.com 

 

 

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"Advancells is a strong advocate of greater transparency in medical procedures in general and Stem Cells Procedures in particular. As a part of our effort of bringing transparent procedures to our clients, we provide each client a Third Party Certificate (from an internationally accredited lab) for the cell count and viability of the cells that we are able to process from the autologous cell source of the patient. To view the sample copy of the certificate  "click here"

 

 

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