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Genetic diseases, such as hemophilia.
It is the treatment of genetic disorders/diseases by altering the person's genotypes.
It eliminates the undesired gene and replaces it with a unaffected gene
There are a number of factors which have kept gene therapy from becoming an effective treatment for genetic disease. The viral rectors are the main problems which might make gene therapy to cause diseases.
Eve K. Nichols has written: 'Human gene therapy' -- subject(s): Gene therapy, Genetic intervention, Government policy, Hereditary Diseases, Moral and ethical aspects, Moral and ethical aspects of Gene therapy, Therapy, Genetic Intervention
Gene therapy is not always successful. Sometimes when inserting genes into the chromosome, we misplace them, and the original problem is aggravated. Gene therapy can be somewhat effective at reducing symptoms of genetic diseases though.
Gene therapy may be performed to treat genetic disorders caused by mutations in a person's DNA. It can involve introducing a functional copy of the gene into the cells to restore normal function. Gene therapy holds the potential to provide long-term or permanent solutions to genetic diseases.
Gene Therapy
Cystic fibrosis and muscular dystrophy. There are perhaps more.
That process is called gene therapy. It involves inserting functional copies of a gene into the cells of a person with a genetic disorder to correct the genetic mutation causing the disorder.
Because scientists want to see what they can do to help people in need of medical attention because of the hereditary diseases they may have. Gene therapy also has the potential to provide permanent cures for diseases as opposed to temporary alleviations of the symptoms or deficiencies.
Gene therapy is a method that aims to cure inherited diseases by providing the patient with correct copy of the defective gene. There are four potential approaches to gene therapy:1)Addition of normal gene to replace the function of defective gene. This is gene replacement orgene augmentation therapy.2)Replacing the defective gene with the correct gene. This isCorrective gene therapy.3)Establishment of alternative pathways that bypass mutant genes function4)Change in regulation of normal or mutant genesThe first two are the basic approaches in gene therapy