About Lysosomal Storage Diseases

Lysosomal storage diseases (LSDs) refer to a group of diseases arising because of the deficiency of lysosomal enzymes, which leads to the accumulation of partially digested or undigested macromolecules inside the cell. LSDs includes progressive diseases with variable ages of onset and clinical symptoms. LSDs are autosomal recessive disorders that are passed on from generation to generation. However, Fabry disease and MPS II are X-linked recessive disorders, which are inherited through mutated alleles on X chromosome.

Covered in this report

The report covers the present scenario and the growth prospects of the global lysosomal storage diseases market for 2017-2021. The report presents a detailed picture of the market by way of study, synthesis, and summation of data from multiple sources.

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The global lysosomal storage diseases market to grow at a CAGR of 7.43% during the period 2017-2021.

The market is divided into the following segments based on geography:

• Americas

• APAC

• EMEA

Global Lysosomal Storage Diseases Market 2017-2021, has been prepared based on an in-depth market analysis with inputs from industry experts. The report covers the market landscape and its growth prospects over the coming years. The report also includes a discussion of the key vendorsoperating in this market.

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Market driver

• Unmet medical needs

• For a full, detailed list, view our report

Market challenge

• Expensive treatment regimen for LSDs

• For a full, detailed list, view our report

Key vendors

• Actelion Pharmaceuticals

• BioMarin

• Genzyme

• Shire

Other prominent vendors

• Alexion Pharmaceuticals

• Amicus Therapeutics

• Chiesi Farmaceutici

• Greenovation Biotech and FGK Clinical Research

• Horizon Pharma

• Leadiant Biosciences

• Mylan

• Pfizer

• Protalix

• Raptor

• Recordati

• Synageva BioPharma

• Valerion Therapeutics

• Vtesse

Market trend

• Regulatory assistance in emerging nations

• For a full, detailed list, view our report

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