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Possible treatments of Huntington’s disease: a comprehensive review

bracu.degree.levelUndergraduate
bracu.type.groupStudent Works
datacite.rightsOpen Access
dc.contributor.advisorHaque, Md. Aminul
dc.contributor.authorLopa, Sadia Zaman
dc.contributor.departmentSchool of Pharmacy
dc.date.accessioned2025-01-12T06:54:51Z
dc.date.available2025-01-12T06:54:51Z
dc.date.copyright©2022
dc.date.copyright2022
dc.date.issued2022-12
dc.descriptionCataloged from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 31-33).
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022.en_US
dc.description.abstractHuntington's disease (HD) is characterized by chorea, cognitive impairment, and behavioral problems; it is a hereditary, progressive neurological condition. HD is becoming easier to diagnose and learn about, but it is still tricky to treat due to severe symptoms and a lack of authorized therapeutic approaches. Both non pharmacologic and pharmacologic approaches have been studied, with more than 80 medicines from different classes having been the subject of clinical trials or case reports. However, antidopaminergic drugs are typically only used to treat motor dysfunction while antidepressants are used to treat mood problems, leaving cognitive impairment untreated. Clinical trials have focused on multiple potential mechanisms for altering symptoms and disease progression.en_US
dc.description.degreeBachelor of Pharmacy
dc.description.statementofresponsibilitySadia Zaman Lopa
dc.format.extent45 pages
dc.identifier.otherID 18346034
dc.identifier.urihttp://hdl.handle.net/10361/25115
dc.language.isoenen_US
dc.publisherBRAC Universityen_US
dc.rightsBrac 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.subjectHuntington's diseaseen_US
dc.subjectNeurodegenerative disorderen_US
dc.subjectAntidepressantsen_US
dc.subjectAntidopaminergic drugsen_US
dc.subjectInherited disorderen_US
dc.subjectGenetic disorderen_US
dc.subject.lcshHuntington's disease--Treatment.
dc.subject.lcshNervous system--Diseases--Treatment.
dc.subject.lcshNervous system--Degeneration.
dc.titlePossible treatments of Huntington’s disease: a comprehensive reviewen_US
dc.typeThesisen_US

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