(Albany, US) DelveInsight has launched a new report on “Sialidosis Market Insights, Epidemiology, and Market Forecast-2030“.
DelveInsight’s “Sialidosis Market Insights, Epidemiology, and Market Forecast-2030″ report delivers an in-depth understanding of the Sialidosis , historical and forecasted epidemiology as well as the Sialidosis market trends in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan.
Some of Sialidosis facts:
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Scope of Sialidosis Report:
Sialidosis is characterized by a deficiency of the digestive enzyme, alpha-neuraminidase. The lack of this enzyme results in an abnormal accumulation of complex carbohydrates known as mucopolysaccharides, and of fatty substances known as mucolipids. Both of these substances accumulate in bodily tissues. There are four types of Sialidosis: Each type of Sialidosis is characterized by the age of onset and by the type of physical and mental manifestations of this disorder.
Type I is the mildest form of Sialidosis, with a range of onset from anywhere between 8-25 years of age. Many of the characteristic features of lysosomal storage diseases including coarse facial features, hepatosplenomegaly (large liver and/or spleen), and dysostosis multiplex (abnormal bone formation that is found in multiple bones of the body) are absent.
One presenting feature is cherry red spots on ophthalmology evaluation. Cherry red spots are spots on the retina that have storage of sugar chain, causing the remainder of the healthy retina to look brighter. Other presenting features include seizures, myoclonus (quick, non- rhythmic muscle contractions that can occur in any skeletal muscle) and other symptoms of nervous system dysfunction.
Type II Sialidosis has an earlier age of onset and more severe symptoms than type I. The congenital form of type II Sialidosis has an onset before birth and symptoms will be present in the newborn period. Often, these babies have hydrops (accumulation of fluid in the body) and do not survive the newborn period. Individuals that survive typically have mental retardation and severe hepatosplenomegaly. Facial features are coarse and dysostosis multiplex is present.
The infantile form of type II Sialidosis has an onset within the first year of life. These individuals have mental retardation, coarse facial features, dysostosis multiplex, and cherry red spots. Hepatosplenomegaly may be present. Unique to the infantile type is renal involvement that may range from structural to functional kidney problems.
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Table of Contents:
1. Key Insights
2. Executive Summary of Sialidosis
3. Competitive Intelligence Analysis for Sialidosis
4. Sialidosis : Market Overview at a Glance
5. Sialidosis : Disease Background and Overview
6. Patient Journey
7. Sialidosis Epidemiology and Patient Population
8. Treatment Algorithm, Current Treatment, and Medical Practices
9. Unmet Needs
10. Key Endpoints of Sialidosis Treatment
11. Marketed Products
12. Emerging Therapies
13. Sialidosis : Seven Major Market Analysis
14. Attribute analysis
15. 7MM: Market Outlook
16. Access and Reimbursement Overview of Sialidosis
17. KOL Views
18. Market Drivers
19. Market Barriers
20. Appendix
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About DelveInsight
DelveInsight is a premier Business Consulting and Market Research firm, focused exclusively on the life science segment. With a wide array of smart end-to-end solutions, the firm helps the global Pharmaceutical, Bio-Tech and Medical devices companies formulate prudent business decisions for improving their performances to stay ahead of the competitors.
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