Treatment of Genetic Disorders
Gene therapy is hoped to cure or improve treatment of genetic disorders by replacing the mutated or malfunctioned gene, manipulating or turning off the gene causing the disease or stimulate other bodily functions to fight the disease. The most common method is replacement of a malfunctioned or sometimes a missed gene with a healthy one. However, gene therapy poses a risk of potentially serious complications, in the first place due to the method that is used to insert the “new” genes – the use of viruses. These have the ability to identify certain cells as well as to transmit the genetic material into the cells containing malfunctioned or missed gene. For that reason modified viruses are used as vectors or carriers of the healthy genes. This method of insertion of healthy genes may not seem problematic at a first glance but it can cause potentially serious complications as already mentioned earlier.
- Inborn Errors of Metabolism
- Chromosomes or DNA
- Genetic factors
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Treatment of Genetic Disorders Conference Speakers
Recommended Sessions
- Advances in Precision Diagnostics
- Drug Target Discovery and Integration
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- Trauma Management - ACEMAC 2026 (France)
- Trauma Surgery and Critical Care - ACEMAC 2026 (France)
- Type 1 & Type 2 Diabetes: Pathogenesis and Management - ENDOCRINOLOGY MEET 2026 (Japan)
- Women Reproductive Cancers - PCOS CONGRESS 2026 (UK)
- Workshops & Special Sessions - traditionalplantmedicine2026 (Japan)