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Stem Cell Therapy for Muscular Dystrophy

Muscular dystrophy (MD) is a group of genetic disorders characterized by progressive muscle weakening and loss, often leading to significant disability and a reduced quality of life. While MD has no definitive cure, emerging therapies, particularly stem cell therapy, offer hope. Stem cell therapy is a field of regenerative medicine that leverages the unique properties of stem cells to repair or replace damaged tissues.

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Stem Cell Therapy for Muscular Dystrophy

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  1. Stem Cell Care India Stem Cell Therapy for Muscular Dystrophy

  2. Understanding Muscular Dystrophy and Its Challenges Muscular dystrophy encompasses various types, including Duchenne muscular dystrophy (DMD), Becker muscular dystrophy, and limb-girdle muscular dystrophy. These diseases typically result from mutations that disrupt the production of essential muscle proteins, like dystrophin in DMD, leading to muscle deterioration. As muscles degenerate, patients face a growing list of challenges, including loss of mobility, respiratory complications, and cardiac issues. Managing MD often requires multidisciplinary care, and even then, conventional treatments only address symptoms without halting disease progression.

  3. Dealing With Muscular Dystrophy Mutations in genes that generate proteins necessary for muscle function cause muscular dystrophy. With DMD, the dystrophin protein—which gives muscle cells structural support—is either absent or inadequate. This causes gradually increasing muscle injury and inflammation over time. Usually diagnosed in early childhood, the illness causes trouble walking, frequent falls, and in later phases respiratory and heart problems.

  4. Stem Cell Treatment Is What? Stem cells are special in that they can grow into several kinds of bodily cells. They could fix broken tissue, create fresh cells, and replace disease-related lost cells. While adult stem cells are more limited in their range but still have great therapeutic promise, embryonic stem cells—which can develop into any cell type—have two major forms. Stem cell treatment aims to substitute healthy, defective or absent muscle cells in the framework of muscular dystrophy. These stem cells can possibly slow down disease progression, enhance muscle function, and rebuild muscle tissue.

  5. Types of Stem Cells in MD Therapy • Mesenchymal Stem Cells (MSCs): • Derived from bone marrow, fat, and other tissues. • Role: Promote tissue repair, reduce inflammation. • Induced Pluripotent Stem Cells (iPSCs): • Created by reprogramming adult cells. • Role: Can become muscle cells and create disease models. • Myogenic Progenitor Cells: • Specialized for muscle formation. • Role: Directly involved in muscle regeneration.

  6. How Stem Cell Therapy Treatments Muscular Dystrophy? Usually involving injecting healthy stem cells into the patient's body to rebuild damaged muscle tissue, stem cell treatment for muscular dystrophy Several methods are under investigation: ● Found in bone marrow, fat, and umbilical cord tissue, mesenchymal stem cells (MSCs) are adult stem cells. By lowering inflammation and pushing new muscle cell development, they have shown promise in healing injured muscle fibers. MSCs also release growth factors meant to aid in muscle injury healing. ● Adult cells called induced pluripotent stem cells (iPSCs) have been genetically reprogrammed to resemble embryonic stem cells. Muscle cells among other kinds of cells can be produced from them. Healthy, dystrophin-producing muscle cells made from iPSCs could be transplanted into individuals suffering from muscular dystrophy. ● Natural occurring in muscle tissue, satellite cells are a type of stem cell that help in muscle regeneration following damage. In those with muscular dystrophy, satellite cells either are deficient or malfunctioning. Stem cell treatment is being investigated by researchers as means of enhancing satellite cell performance to boost muscle regeneration. 

  7. Conclusion By treating muscular dystrophy at its genetic and biological bases, stem cell Treatment for Muscular Dystrophy presents a breakthrough approach. Although more studies and clinical trials are required to completely grasp its possibilities, patients and their families have hope based on current development. As stem cell research advances, the future might bring a transforming answer for people afflicted by this crippling disorder.

  8. CONTACT US 8743024344 info@stemcellcareindia.com www.stemcellcareindia.com

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