Muscular Dystrophy Treatment
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Muscular Dystrophy Stem Cell Treatment
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, due to recent successful therapeutic benefits of stem cell therapy for muscular dystrophy treatment, 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 Treatment: 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 muscle weakness treatment solution that is best suited for individual requirements of people undergoing Muscular Dystrophy stem cell treatment.
With extensive research these challenges are now comprehensible to therapeutic ventures resulting in new treatments of muscular dystrophy using autologous treatment/allogenic transplant for adipose-derived mesenchymal stromal cells treatment and bone marrow stromal cells treatment.
This new insight on the treatment of muscular dystrophy has helped in identifying the potential to overcome muscular dystrophy with stem cells, primarily using autologous stem cell transplant in form of hematopoietic stem cell transplant or mesenchymal stromal cells treatment.
Stem Cell Therapy for Muscular Dystrophy Treatment at Advancells is divided into 4 Steps
Processing of stem cells
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 Stem Cell Treatment
What is Muscular Dystrophy (MD)? Muscular Dystrophy (MD) is a collection of inherited muscular degeneration diseases that damage and weaken the muscles progressively. The lack of dystrophin, a protein required for normal muscle function, is responsible for the damage....
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...
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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 muscle weakness treatment. 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
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