Molecular Cytogenetics Of Myelodysplastic Syndrome – Hospital Based Study

dc.contributor.authorIsa, Asmida
dc.date.accessioned2019-07-12T02:05:58Z
dc.date.available2019-07-12T02:05:58Z
dc.date.issued2014-07
dc.description.abstractMyelodysplastic Syndrome (MDS) is a haematological condition characterised by hypercellular bone marrow and low peripheral blood counts. The objectives of this study were to identify chromosomal aberration using conventional cytogenetics and array comparative genomic hybridisation (array-CGH) in MDS patients and correlate with its’ haematological findings. A total of 8 patients were recruited. Cytogenetic results revealed six normal karyotypes, a karyotype with structural abnormalities (del(5)(q13q33) and a karyotype with complex rearrangement (t(1;11), t(2;11), del(4p), del(5p), del(9p)). By array-CGH technique, known cytogenetic aberrations, complex chromosome aberrations and rare/cryptic aberrations (<5 Mb) were detected. In the case of common aberrations, del5q (q13.1 - q13.2 (2.4 Mb)) and large amplification of chromosome 8 (p23.3-p11.1 (46.3 Mb) and q11.1-q24.3 (98.7 Mb)) were detected. In complex aberrations, the aberrations involved from 0.7 Mb to 98.7 Mb in size. These patients showed similarities of haematological findings. Five cryptic aberrations were identified in 3 patients (0.7 Mb to 4.8 Mb). As a conclusion, common, complex and cryptic aberrations were detected in MDS patients. The associated haematological findings could provide useful information to stratify the suitability of the treatments for the patients. These findings also might contribute to the heterogeneity of choromosomal aberrations in MDS patients.en_US
dc.identifier.urihttp://hdl.handle.net/123456789/8469
dc.language.isoenen_US
dc.publisherUniversiti Sains Malaysiaen_US
dc.subjectMolecular cytogenetics ofen_US
dc.subjectmyelodysplastic syndromeen_US
dc.titleMolecular Cytogenetics Of Myelodysplastic Syndrome – Hospital Based Studyen_US
dc.typeThesisen_US
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