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dc.contributor.editorOppezzo, Pablo
dc.date.accessioned2021-04-20T15:20:00Z
dc.date.available2021-04-20T15:20:00Z
dc.date.issued2012
dc.identifierONIX_20210420_9789533078816_904
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/65547
dc.description.abstractB-cell chronic lymphocytic leukemia (CLL) is considered a single disease with extremely variable course, and survival rates ranging from months to decades. It is clear that clinical heterogeneity reflects biologic diversity with at least two major subtypes in terms of cellular proliferation, clinical aggressiveness and prognosis. As CLL progresses, abnormal hematopoiesis results in pancitopenia and decreased immunoglobulin production, followed by nonspecific symptoms such as fatigue or malaise. A cure is usually not possible, and delayed treatment (until symptoms develop) is aimed at lengthening life and decreasing symptoms. Researchers are playing a lead role in investigating CLL's cause and the role of genetics in the pathogenesis of this disorder. Research programs are dedicated towards understanding the basic mechanisms underlying CLL with the hope of improving treatment options.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJD Cardiovascular medicineen_US
dc.subject.otherMusculoskeletal medicine
dc.titleChronic Lymphocytic Leukemia
dc.typebook
oapen.identifier.doi10.5772/1156
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9789533078816
oapen.relation.isbn9789535167464
oapen.imprintIntechOpen
oapen.pages464


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