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- Advances in Duchenne Muscular Dystrophy TreatmentCauses and Mechanism of Duchenne Muscular Dystrophy Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is caused by the absence of dystrophin, a protein that helps keep muscle cells intact. The defective gene that causes DMD is located on the X chromosome, so it primarily affects boys. Girls can be carriers of the defective...0 Commentaires 0 Parts 371 Vue
- Collaboration and Innovation: How Excelra and Lantern Pharma Are Tackling Rare Diseases with Repurposed DrugsIn recent years, several key players in the pharmaceutical industry have driven advancements in drug repurposing through innovative technologies and strategic partnerships. Companies such as Algernon Pharmaceuticals, Fios Genomics, Excelra, Lantern Pharma, and Teva Pharmaceutical Industries are leveraging cutting-edge solutions like AI and machine learning,...0 Commentaires 0 Parts 202 Vue
- Erythromelalgia Treatment Options for Managing Pain SymptomsPathophysiology and Causes of Erythromelalgia Erythromelalgia is a rare medical condition characterized by episodic burning pain, redness, and increased skin temperature in the extremities, usually the feet and hands. The exact cause of erythromelalgia is unknown, but it involves abnormalities in the nervous system and blood vessels that lead to increased blood flow to the skin and subsequent...0 Commentaires 0 Parts 142 Vue
- Exploring Global Initiatives in NPHP5 Retinal Degeneration TreatmentIn recent years, significant strides have been made in understanding and treating NPHP5 retinal degeneration on a global scale. This inherited retinal disorder, characterized by progressive vision loss, affects individuals worldwide, prompting concerted efforts in research and treatment development. Let's delve into the multifaceted approaches and innovations driving the quest for effective...0 Commentaires 0 Parts 761 Vue
- Exploring the Landscape of Leigh Syndrome Treatment: Insights and ConsiderationsLeigh Syndrome Treatment encompasses a diverse array of approaches aimed at managing the symptoms and complications associated with this rare and debilitating neurological disorder. With Leigh Syndrome being a genetic condition characterized by mitochondrial dysfunction, treatment strategies focus on alleviating symptoms, improving quality of life, and addressing the underlying molecular...0 Commentaires 0 Parts 593 Vue
- Global Leigh Syndrome Treatment Market is Estimated to Witness High Growth Owing to Advancement in Gene TherapyThe global Leigh syndrome treatment market is witnessing high growth owing to the advancement in gene therapy. Leigh syndrome is a rare neurological genetic disorder that affects the central nervous system and metabolism. It is usually seen in infants and children under the age of 2. The signs and symptoms associated with Leigh syndrome include poor muscle tone, muscle weakness, vision issues,...0 Commentaires 0 Parts 679 Vue
- How Major Players are Using Machine Learning to Redefine Drug Repurposing for Rare DiseasesWhat Drugs Are Being Repurposed for Alzheimer's Treatment? Alzheimer's disease poses significant challenges due to its complex pathophysiology and the lack of effective treatments. Recent studies have explored repurposing existing drugs to find new therapeutic options. Algernon Pharmaceuticals is investigating Dextromethorphan, a common cough suppressant, for its potential...0 Commentaires 0 Parts 177 Vue
- Rare Disease Genetic Testing Market Emerging Technologies, Competitive Landscape, Future Plans and Forecast to 2032"According to the research report, the global rare disease genetic testing market was valued at USD 886.6 million and is expected to reach USD 3,102.4 million by 2032, to grow at a CAGR of 13.4% during the forecast period." A recently published report titled Rare Disease Genetic Testing Market Regional Overview, Business Strategies and Industry Size Forecast to 2032 by Polaris Market...0 Commentaires 0 Parts 724 Vue
- Rare Disease Genetic Testing Market Market: Size, Drivers, Trends, Competitor Insights 2024-2032“According to the research report, the global rare disease genetic testing market was valued at USD 334.7 million in 2023 and is expected to reach USD 3,102.4 million by 2032, to grow at a CAGR of 12.70% during the forecast period.” Polaris Market Research announces the release of its latest report on Rare Disease Genetic Testing Market 2024: By Types, Applications, Size, Share,...0 Commentaires 0 Parts 410 Vue
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