dc.contributor.advisor | Sayka Khan, Tanisha Tabassum | |
dc.contributor.author | Tanjum, Atia | |
dc.date.accessioned | 2024-04-24T04:54:01Z | |
dc.date.available | 2024-04-24T04:54:01Z | |
dc.date.copyright | 2022 | |
dc.date.issued | 2022-10 | |
dc.identifier.other | ID: 15346034 | |
dc.identifier.uri | http://hdl.handle.net/10361/22661 | |
dc.description | This thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022. | en_US |
dc.description | Cataloged from PDF version of thesis. | |
dc.description | Includes bibliographical references (pages 54-58). | |
dc.description.abstract | Genetic disorders are widespread. However, many of these genetic illnesses have minimal
information, making therapy difficult. Gene therapy has emerged as a major breakthrough in
the field of medical science to treat diseases resulting from defective genes. The FDA has
received over 900 gene therapies for hereditary disorders. Rare genetic illnesses are life threatening and impact 5 per 10000 people worldwide. Researchers are conducting clinical
trials to investigate treatments for rare genetic disorders despite a paucity of knowledge. With
sufficient clinical trial data showing signs of improvement among the patients and safety of
gene delivery systems, gene therapy can be the most efficient treatment strategy for rare genetic
disorders. In this review paper, a number of rare genetic disorders and the prospects of gene
therapy in the treatment of those disorders were discussed. | en_US |
dc.description.statementofresponsibility | Atia Tanjum | |
dc.format.extent | 58 pages | |
dc.language.iso | en | en_US |
dc.publisher | Brac University | en_US |
dc.rights | Brac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. | |
dc.subject | Gene therapy | en_US |
dc.subject | Vectors | en_US |
dc.subject | Rare genetic disorders | en_US |
dc.subject | Clinical trial | en_US |
dc.subject.lcsh | Gene therapy. | |
dc.subject.lcsh | Genetic disorders. | |
dc.subject.lcsh | Genetic disorders--Treatment. | |
dc.title | Gene therapy for rare genetic disorders | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | School of Pharmacy, Brac University | |
dc.description.degree | B. Pharmacy | |