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Hunter Syndrome Treatment Market To Grow Steadily by 2030

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Michael Jaikishan
Hunter Syndrome Treatment Market To Grow Steadily by 2030

According to the National Institute of Health 2018 report, frequency of MPS II is 1 in 100,000 to 1 in 160,000 in males. Hunter syndrome is of two types, severe and mild. These both affect numerous different tissues and organs. Individuals with extreme case begin to lose basic functional skills between the age group of 6 and 8 years. The normal life expectancy of these people is 10 to 20 years.


Data Bridge Market Research analyses a growth rate in the Hunter syndrome treatment market in the forecast period 2023-2030. The expected CAGR of schistosomiasis diseases market is tend to be around 8.6% in the mentioned forecast period. The market was valued at USD 927.57 million in 2022, and it would grow up to USD 1794.67 million by 2030. In addition to the market insights such as market value, growth rate, market segments, geographical coverage, market players, and market scenario, the market report curated by the Data Bridge Market Research team also includes in-depth expert analysis, patient epidemiology, pipeline analysis, pricing analysis, and regulatory framework.


Hunter syndrome is a rare, inherited genetic disorder that is caused by missing or malfunctioning of enzyme, iduronate-2-sulfatase. Body does not properly digest or break down sugar molecules in the body. When these molecules build up in organs and tissues over the time, they can cause severe damage, affecting physical and mental development and abilities. The disorder commonly occurs in boys. The condition is one of a group of inherited metabolic disorders known as mucopolysaccharidosis (MPS).


Read Full Report Summary @ https://www.databridgemarketresearch.com/reports/global-hunter-syndrome-treatment-market


North America is dominating the market due to the presence of key product manufacturers and increasing research and development activities. Asia-Pacific is considered to grow over the coming years due to increasing investment in innovative R&D for novel treatment product.


Key players operating in the Hunter syndrome treatment market include:

Takeda Pharmaceutical Company Limited (Japan)

F. Hoffmann-La Roche Ltd (Switzerland)

Abbott (U.S.)

Medtronic (Ireland.)

Abbott (U.S.)

BD (U.S.)

Johnson & Johnson Services, Inc.(U.S.)

GSK Plc. (U.K.)

Bayer AG (Germany)

Zimmer Biomet (U.S.)

Stryker Corporation (U.S.)

Homology Medicines, Inc (U.S.)

Novartis AG (Switzerland)

Pfizer Inc.(U.S.)

JCR Pharmaceuticals Co., Ltd. (Japan)

Sangamo Therapeutics (U.S.)

AVROBIO, Inc (U.S.)

REGENXBIO Inc (U.S)

CANbridge Life Sciences Ltd. (Taiwan)

Denali Therapeutics (U.S.)

Jasper Therapeutics, Inc. (U.S.)


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