The 7 major Angelman syndrome markets reached a value of US$ 105.1 Million in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 165.6 Million by 2034, exhibiting a growth rate (CAGR) of 4.22% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year |
2023
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Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 105.1 Million |
Market Forecast in 2034
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US$ 165.6 Million |
Market Growth Rate 2024-2034 | 4.22% |
The Angelman syndrome market has been comprehensively analyzed in IMARC's new report titled "Angelman Syndrome Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Angelman syndrome is a complex genetic condition that affects the nervous system. The disorder is mainly caused by mutations in the UBE3A gene in chromosome region 15, which is responsible for producing proteins involved in the development and maintenance of various organs in the body. Angelman syndrome is characterized by intellectual disability or severe developmental delay, speech impairment, tremulousness of the limbs and/or gait ataxia, microcephaly (small head size), recurrent seizures, etc. Some of the common symptoms associated with this ailment include trouble sleeping, hand-flapping movements, unique behavior with frequent smiling, laughing, excitability, etc. The diagnosis of Angelman syndrome typically involves a combination of clinical evaluation, medical history, and genetic testing. Physicians may perform a physical exam to look for characteristic features of the condition, such as hypopigmented skin and eyes and abnormal side-to-side spine curvature. Blood and gene tests are used to detect genetic mutations associated with the disease. Additionally, radiographic examinations, including brain MRI and CT scans, can confirm the diagnosis of the ailment. In some cases, various DNA methylation studies are also utilized to evaluate the chromosome defects that cause the disorder.
The increasing cases of genetic disorders and the rising unmet need for effective treatments to address the underlying congenital defect and improve patient outcomes are primarily driving the Angelman syndrome market. In addition to this, the widespread utilization of novel medications, including anticonvulsants, mild laxatives, sedatives, etc., to reduce the symptoms of the condition is creating a positive outlook for the market. Moreover, the escalating adoption of electroencephalogram (EEG), which measures abnormal brain activity with a characteristic pattern of large-amplitude slow-spike waves to diagnose seizures or other neurological problems associated with Angelman syndrome, is further bolstering the market growth. Apart from this, the emerging popularity of CRISPR gene editing technology, which can override the DNA mutations underlying Angelman syndrome, is acting as another significant growth-inducing factor. Furthermore, several key players are making extensive investments in achieving a better understanding of the natural history of the ailment, including the course of disease progression and factors that influence outcomes, for creating novel treatments. This, in turn, is also augmenting the market growth. Additionally, the ongoing development of antisense oligonucleotide therapeutics for providing targeted and long-lasting effects, with the possibility of disease modification rather than just symptom relief, is expected to drive the Angelman syndrome market during the forecast period.
IMARC Group's new report provides an exhaustive analysis of the Angelman syndrome 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 Angelman syndrome 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 Angelman syndrome 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 Angelman syndrome marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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ION582 | Ionis Pharmaceuticals |
GTX 102 | Ultragenyx Pharmaceutical Inc |
NNZ-2591 | Neuren Pharmaceuticals |
RO 7248824 | Roche |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
Angelman Syndrome: Current Treatment Scenario, Marketed Drugs and Emerging Therapies