Hutchinson-Gilford Progeria Treatment Market Lucrative Opportunities Till 2026

Hutchinson-Gilford
Progeria
Treatment
Market Size, Share, Trend, Outlook, Future
Analysis And Synthesis By 2026
Hutchinson-Gilford progeria syndrome is a genetic condition characterized by the dramatic, rapid,
appearance of aging from the childhood. Hutchinson-Gilford progeria syndrome is caused by a mutation
in the lamin A (LMNA) gene. The affected children develop a characteristic facial experience including
prominent eyes, small chin, protruding ears, thin lips and a thin nose with a beaked tip. This syndrome
also causes hair loss (alopecia), joint abnormalities, aged-looking skin, and a loss of fat under the skin
(subcutaneous fat). Moreover, patients of Hutchinson-Gilford progeria syndrome experiences severe
hardening of the arteries (arteriosclerosis) from the childhood. The condition worsens with age and
increases the risk of heart attack or stroke even at a young age.
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Hutchinson-Gilford progeria is a rare condition that affects about one in four million newborns
worldwide according to the National Institutes of Health (NIH). Until now more than 130 cases have
been reported as per the NIH statistics. The affected patients live up to 30 years maximum, with an
average life span of 13 years. Nearly 90% of the patients die from complications related to
atherosclerosis. Till 2012 there wasn’t any effective treatment therapy discovered for Hutchinson-Gilford
progeria syndrome. The treatments available focused mostly on reducing cardiovascular symptoms and
growth abnormalities.
Farnesyltransferase Inhibitor (FTI)
In 2012, findings of the first clinical trial of the drug Lonafarnib, a farnesyltransferase inhibitor
(FTI), gave a new hope for the treatment of children with Hutchinson-Gilford progeria
syndrome. Clinical trial results demonstrated improvement in weight gain, increase in bone
mineral density, reduced vascular stiffness, and improved sensorineural hearing in patients with
progeria. Previous treatments with growth hormone, and Sulforaphane helped in reducing the
symptoms, and prolong a child’s life. However, it is essential that the patient regularly visits
the cardiologist. Rapamycin is one other drug used before, that demonstrated to reverse nuclear
blebbing, retard cellular senescence, and facilitate degradation of progerin.
Report includes chapters which deeply display the following deliverable about industry :
• Hutchinson-Gilford Progeria Treatment Market Research Objective and Assumption
• Hutchinson-Gilford Progeria Treatment Market Purview - Report Description, Executive
Summary, and Coherent Opportunity Map (COM)
• Hutchinson-Gilford Progeria Treatment Market Dynamics, Regulations, and Trends Analysis Market Dynamics, Regulatory Scenario, Industry Trend, Merger and Acquisitions, New system
Launch/Approvals, Value Chain Analysis, Porter’s Analysis, and PEST Analysis
• Global Hutchinson-Gilford Progeria Treatment Market, By Regions
• Hutchinson-Gilford Progeria Treatment Market Competition by Manufacturers including
Production, Share, Revenue, Average Price, Manufacturing Base Distribution, Sales Area and
Product Type.
• Hutchinson-Gilford Progeria Treatment Market Manufacturers Profiles/Analysis including
Company Basic Information, Manufacturing Base and Its Competitors.
• Hutchinson-Gilford Progeria Treatment Market Manufacturing Cost Analysis including Key Raw
Materials and Key Suppliers of Raw Materials.
• Industrial Chain, Sourcing Strategy and Downstream Buyers including Upstream Raw Materials
Sourcing and Downstream Buyers
• Marketing Strategy Analysis, Distributors/Traders including Marketing Channel, Market
Positioning and Distributors/Traders List.
• Market Effect Factors Analysis including Technology Progress/Risk, Consumer Needs/Customer
Preference Change and Economic/Political Environmental Change.
• Hutchinson-Gilford Progeria Treatment Market Forecast including Production, Consumption,
Import and Export Forecast by Type, Applications and Region.
• Research Findings and Conclusion
Recently in 2015, the scientists at the Agency for Science, Technology & Research (A*STAR) successfully
established a model of Hutchinson-Gilford progeria syndrome. The study conducted by this organization
proposed a model which implies that progerin is linked to telomeres. Progerin induces a reduction in
heterochromatin, a tightly packed form of DNA, making telomeres in the cell more fragile and
susceptible to damage. The damaged telomeres in turn trigger premature cellular aging. This model is
radically different from the one believed earlier – the gene progerin caused the nucleus to be deformed,
thereby weakening the ability of cells to divide and proliferate. The altered progerin protein makes the
nuclear envelope unstable and progressively damages the nucleus, making cells more likely to die
prematurely.
Researchers are working to determine how genetic changes further leading to the characteristic features
of Hutchinson-Gilford progeria syndrome. Continuous advancement in research with increased
understanding of the human aging will provide valuable insights and aid in the treatment of this
disease.
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Continuous advancement in research with increased understanding of the human aging will provide valuable insights and aid in the treatment of this disease.