Lysosomal storage diseases

dc.contributor.authorAdenegan, Adesola Idowu
dc.date.accessioned2012-11-30T08:17:48Z
dc.date.available2012-11-30T08:17:48Z
dc.date.issued2012-11-30
dc.descriptionIndividually, lysosomal storage disorders are rare genetic diseases. However, as a group, they are relatively common and represent an important health problem. Their early diagnosis is paramount since there are increasing possible therapies even though majority are still going through clinical trials.uk_UK
dc.description.abstractLysosomes are subcellular organelles responsible for the physiologic turnover of cell constituents. Lysosomal storage diseases describe a heterogeneous group of dozens of rare inherited disorders characterized by the accumulation of undigested or partially digested macromolecules, which ultimately results in cellular dysfunction and clinical abnormalities. Several studies have explored different methods of treatment, but only are promising and safe even though they are very expensive.uk_UK
dc.identifier.citationAdenegan Adesola Idowu. Lysosomal storage diseases [Electronic resource] : [presentation PowerPoint] / Adesola Idowu Adenegan. – Electronic data (19 slides). – Kharkiv, 2012.
dc.identifier.urihttps://repo.knmu.edu.ua/handle/123456789/2045
dc.language.isoenuk_UK
dc.titleLysosomal storage diseasesuk_UK
dc.typePresentationuk_UK

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