Del11q(13) Is A Rare Cytogenetic Abnormality In Acute Myeloid Leukemia

EMİNE GÖKTAŞ, AYŞEGÜL ZAMANİ, AYNUR UĞUR BİLGİN, MAHMUT SELMAN YILDIRIM

  • Year : 2016
  • Vol : 32
  • Issue : 4
  •  Page : 88-90
Acute myeloid leukemia is the most common type seen in adults with 3-4/100000 incidence and accounting for %20 newly diagnosed patients each year. Patient may present with a broad variety of symptoms including low-grade fever, easy bruising, anemia, weakness in immune system. Cytogenetic analysis is a key component in diagnostic of acute myeloid leukemia. Chromosomal abnormality is present in the majority of malignant cells in acute myeloid leukemia patients. We presented a rare acute myeloid leukemia case with 46, XX del11q(13) karyotype organization.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
Del11q(13) Is A Rare Cytogenetic Abnormality In Acute Myeloid Leukemia
, Vol. 32 (4)
Received : 16.11.2015, Accepted : 16.11.2015, Published Online : 13.08.2018
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ISSN:1017-6616;
E-ISSN:2149-8059;