Significance of Muscular Dystrophy
Muscular Dystrophy refers to a group of genetic disorders that lead to progressive muscle weakness and degeneration, primarily due to mutations affecting muscle-related proteins like dystrophin. It predominantly affects boys and manifests through muscle atrophy and loss of mass. These hereditary conditions result in increasing disability and may pose life-threatening challenges. While there is currently no cure, potential treatments include therapies such as stem cell therapy and alternative methods like Shastikashali pinda sweda for symptom alleviation.
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The concept of Muscular Dystrophy in scientific sources
Muscular Dystrophy is a group of inherited genetic disorders leading to progressive muscle weakness and degeneration, often exacerbated by X-linked mutations affecting the dystrophin protein, primarily impacting males and resulting in significant disability and health risks.
From: World Journal of Pharmaceutical Research
(1) A group of genetic disorders that result in muscle weakness and loss of muscle tissue.[1] (2) A collection of muscular ailments characterized by degenerative weakness and loss in muscular mass, primarily affecting boys and caused by genetic mutations that hinder protein production essential for muscle structure.[2] (3) A hereditary condition characterized by progressive muscle weakness and atrophy.[3] (4) A collection of muscular ailments characterized by degenerative weakness and loss in muscular mass, affecting a large number of children.[4] (5) A group of genetic diseases causing progressive weakness and loss of muscle mass, which may be addressed through stem cell therapy.[5]
From: International Ayurvedic Medical Journal
(1) A group of diseases characterized by progressive weakness and degeneration of muscle fibers, potentially alleviated by Shastikashali pinda sweda.[6] (2) A group of inherited genetic conditions that progressively weaken muscles, leading to increasing disability and threats to life.[7] (3) A catastrophic heritable condition caused by X-linked neuromuscular disorder due to mutations in the gene containing dystrophin protein, affecting only males, leading to progressive muscle weakness and degeneration.[8]