Duchenne muscular dystrophy is a medical condition that develops due to shortage of protein called “dystrophin”. It causes deterioration and break down of muscles, which results in walking difficulty and limited general mobility. Duchenne muscular dystrophy is considered as one of the most progressive childhood neuromuscular disorders. However, it affects boys mostly, but few cases of girls have been registered too.
Duchenne muscular dystrophy affects around 1 in 3,500 male births worldwide. It is usually identified between the age of three and six. Weakness and wasting (atrophy) of the muscles of the pelvic area characterize duchenne muscular dystrophy and it is followed by the involvement of the shoulder muscles.
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Global Duchenne Muscular Dystrophy Market Witness Most Promising Rise in Demand:
The global duchenne muscular dystrophy market is estimated to gain traction from increased research and development activities, augmented demand for efficacious therapies among patients, and introduction of novel disease therapies. Furthermore, rising prevalence of the disease is projected to propel the global duchenne muscular dystrophy market towards growth.
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The report offers a comprehensive evaluation of the market. It does so via in-depth qualitative insights, historical data, and verifiable projections about market size. The projections featured in the report have been derived using proven research methodologies and assumptions. By doing so, the research report serves as a repository of analysis and information for every facet of the market, including but not limited to: Regional markets, technology, types, and applications.
Key Players of Duchenne Muscular Dystrophy Market Report:
A few of the prominent market players are BioMarin Pharmaceutical Inc., Catabasis Pharmaceuticals Inc., GlaxoSmithKline Plc., Santhera Pharmaceuticals Holding AG, ReveraGen BioPharma Inc., and Akashi Therapeutics Inc.
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