The myotonic dystrophy type 2 market reached a value of USD 45.9 Million across the top 7 markets (US, EU4, UK, and Japan) in 2024. Looking forward, IMARC Group expects the top 7 major markets to reach USD 79.1 Million by 2035, exhibiting a growth rate (CAGR) of 5.28% during 2025-2035.
Report Attribute
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Key Statistics
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---|---|
Base Year | 2024 |
Forecast Years | 2025-2035 |
Historical Years |
2019-2024
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Market Size in 2024
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USD 45.9 Million |
Market Forecast in 2035
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USD 79.1 Million |
Market Growth Rate (2025-2035)
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5.28% |
The myotonic dystrophy type 2 market has been comprehensively analyzed in IMARC's new report titled "Myotonic Dystrophy Type 2 Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2025-2035". Myotonic dystrophy type 2 is a genetic, autosomal dominant condition involving progressive muscle weakness, predominantly affecting muscles close to the middle of the body (proximal muscles). Myotonic dystrophy type 2 is usually a less severe condition than myotonic dystrophy type 1. The clinical presentation of this disease typically happens during the third or fourth decade, and the most frequent symptoms are muscle weakness, stiffness, and pain. The weakness tends to involve the proximal muscles of the shoulders and pelvis and causes trouble climbing stairs, combing and drying hair, and standing up from a chair. The affected persons may also have cardiac conduction defects, posterior subcapsular cataracts, and diabetes. Myotonic dystrophy type 2 is mainly diagnosed by combining clinical history, physical examination, and laboratory work. The health practitioner typically orders genetic testing to detect the existence of the unique genetic sequence causing the condition. In other situations, a muscle biopsy is also conducted to rule out a diagnosis and exclude other potential causes of underlying symptoms.
The escalating prevalence of mutation in the CNBP gene on chromosome 3, resulting in an unstable expansion of a segment of DNA called CCTG, is primarily driving the myotonic dystrophy type 2 market. In addition to this, the inflating utilization of sodium channel blockers, such as mexiletine, tricyclic antidepressants, benzodiazepines, etc., to reduce sustained myotonia and manage the symptoms of the disease is also creating a positive outlook for the market. Moreover, the rising usage of CPAP (continuous positive airway pressure) machine that can be used to treat sleep apnea in individuals with myotonic dystrophy type 2 is further bolstering the market growth. This procedure can help in managing breathing difficulties caused by respiratory muscle weakness associated with the condition. Apart from this, the widespread adoption of physical therapy, which includes tailored exercise programs to maintain muscle strength and range of motion in patients, is acting as another significant growth-inducing factor. Additionally, the emerging popularity of adeno-associated virus (AAV) genetic treatment, since it works by delivering a modified gene to muscle tissue using an AAV vector, aiming to counteract the effects of the genetic mutation causing the disease, is expected to drive the myotonic dystrophy type 2 market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the myotonic dystrophy type 2 market in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report the United States has the largest patient pool for myotonic dystrophy type 2 and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario and unmet medical needs, etc. have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the myotonic dystrophy type 2 market in any manner.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current myotonic dystrophy type 2 marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Market Insights
Epidemiology Insights
Myotonic Dystrophy Type 2: Current Treatment Scenario, Marketed Drugs and Emerging Therapies