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HEREDITARY HEMOCHROMATOSIS AND JAK2-POSITIVE POLYCYTHEMIA VERA
  • Ahmed Radwan,
  • Ibraheem Othman
Ahmed Radwan
University of Saskatchewan
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Ibraheem Othman
Allan Blair Cancer Centre
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Abstract

A 59-year-old male was diagnosed with JAK2-positive Polycythemia Vera. Subsequently, further lab testing revealed elevated ferritin and iron saturation. Genetic testing for HFE gene mutation screen revealed that the patient was positive for heterozygous C282Y mutation. The patient was ultimately diagnosed with both Polycythemia Vera and Hereditary Hemochromatosis.

Peer review status:ACCEPTED

17 Jul 2021Submitted to Clinical Case Reports
21 Jul 2021Submission Checks Completed
21 Jul 2021Assigned to Editor
08 Aug 2021Reviewer(s) Assigned
10 Sep 2021Review(s) Completed, Editorial Evaluation Pending
10 Sep 2021Editorial Decision: Revise Minor
11 Sep 20211st Revision Received
13 Sep 2021Submission Checks Completed
13 Sep 2021Assigned to Editor
13 Sep 2021Review(s) Completed, Editorial Evaluation Pending
21 Sep 2021Editorial Decision: Accept