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Lebers Hereditary Optic Neuropathy Market is Expected to Show a Healthy Growth Rate During the Study Period (2019-2032)| Key Companies-GenSight Biologics, Mitotech

08-07-2023 01:51 PM CET | Health & Medicine

Press release from: DelveInsight Business Research LLP

Lebers Hereditary Optic Neuropathy Market

Lebers Hereditary Optic Neuropathy Market

(Las Vegas, Nevada, United States) "DelveInsight's "Leber Congenital Amaurosis Market Insights, Epidemiology, and Market Forecast-2032" report delivers an in-depth understanding of the Leber Congenital Amaurosis, historical and forecasted epidemiology as well as the Leber Congenital Amaurosis market trends in the United States, EU5 (Germany, Spain, Italy, France, and the United Kingdom) and Japan.
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Lebers Hereditary Optic Neuropathy Overview

Leber hereditary optic neuropathy (LHON) is a rare mitochondrial disorder that typically presents in young males with progressive visual loss due to optic neuropathy. LHON was the first disease to be associated with mitochondrial DNA point mutations and is, therefore, maternally inherited.

Leber Hereditary Optic Neuropathy is transmitted only through the mother, as it is primarily due to mutations in the mitochondrial (not nuclear) genome, and only the egg contributes mitochondria to the embryo. LHON is usually due to one of three pathogenic mitochondrial DNA (mtDNA) point mutations.

Click here to learn more about the Lebers Hereditary Optic Neuropathy Market Landscape @https://www.delveinsight.com/report-store/lebers-hereditary-optic-neuropathy-lhon-market?utm_source=openpr&utm_medium=pressrelease&utm_campaign=dpr

Key Highlight from Leber Hereditary Optic Neuropathy Market Report
In Northern European populations about one in 9,000 people carries one of the three primary Leber Hereditary Optic Neuropathy mutations. There is a prevalence of between 1:30,000 to 1:50,000 in Europe.
The Leber Hereditary Optic Neuropathy mutations ND4 G11778A mutation is the primary mutation in most of the world, with 70% of Northern European cases and 90% of Asian cases. Due to a Founder effect, the LHON ND6 T14484C mutation accounts for 86% of LHON cases in Quebec, Canada.
More than 50% of males with a mutation and more than 85% of females with a mutation never experience vision loss or related medical problems. The particular mutation type may predict the likelihood of penetrance, severity of illness, and probability of vision recovery in the affected. As a rule of thumb, a woman who harbors a homoplasmic primary LHON mutation has a ~40% risk of having an affected son and a ~10% risk of having an affected daughter. Additional factors may determine whether a person develops the signs and symptoms of this disorder. Environmental factors such as smoking and alcohol use may be involved, though studies of these factors have produced conflicting results. Researchers are also investigating whether changes in additional genes, particularly genes on the X chromosome, contribute to the development of signs and symptoms. The degree of heteroplasmy, the percentage of mitochondria that have mutant alleles, may play a role.
Patterns of mitochondrial alleles called haplogroups may also affect the expression of mutations.
Learn more about the treatment market for Lebers Hereditary Optic Neuropathy
https://www.delveinsight.com/report-store/lebers-hereditary-optic-neuropathy-lhon-market?utm_source=openpr&utm_medium=pressrelease&utm_campaign=dpr
The Report Covers the Lebers Hereditary Optic Neuropathy Epidemiology Segmented by:
Lebers Hereditary Optic Neuropathy prevalent cases
Lebers Hereditary Optic Neuropathy incident cases
Lebers Hereditary Optic Neuropathy treatment cases
Lebers Hereditary Optic Neuropathy diagnosed cases
Lebers Hereditary Optic Neuropathy Drug Profile and Companies Covered
GenSight Biologics: EPI-743
Neurophth Therapeutics: Idebenone
Mitotech: Curcumin
Stealth BioTherapeutics: Idebenone
Fortify Therapeutics: rAAV2-ND4
Neuroptika: KH176
And many others.
Learn more about the Key Companies and Emerging Therapies in the Lebers Hereditary Optic Neuropathy Market @ https://www.delveinsight.com/report-store/lebers-hereditary-optic-neuropathy-lhon-market?utm_source=openpr&utm_medium=pressrelease&utm_campaign=dpr
Table of Contents
Key Insights
Kaposi's Sarcoma Introduction
Executive Summary of Lebers Hereditary Optic Neuropathy
Disease Background and Overview
Lebers Hereditary Optic Neuropathy Epidemiology and patient population
Kaposi's Sarcoma Emerging Therapies
Kaposi Sarcoma Market Outlook
Kaposi Sarcoma Market Access and Reimbursement of Therapies
Kaposi Sarcoma Market Drivers
Kaposi Sarcoma Market Barriers
Appendix
Kaposi's Sarcoma Report Methodology
DelveInsight Capabilities
Disclaimer

Learn about the detailed offerings of the Lebers Hereditary Optic Neuropathy Market Outlook report @ https://www.delveinsight.com/report-store/lebers-hereditary-optic-neuropathy-lhon-market?utm_source=openpr&utm_medium=pressrelease&utm_campaign=dpr

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DelveInsight Business Research LLP
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info@delveinsight.com
https://www.delveinsight.com

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

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