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Hemoglobin Wayne Trait with Incidental Polycythemia.
Manju Ambelil1, Nghia Nguyen1, Amitava Dasgupta1
1Department of Pathology and Laboratory Medicine, University of Texas Health Science Center-McGovern Medical School, Houston, TX, USA.
Annals of Clinical and Laboratory Science
|March 3, 2017
Summary
This study identifies a rare hemoglobin Wayne variant in a patient with secondary polycythemia. Diagnostic methods confirmed the variant, crucial for ruling out inherited hemoglobin disorders as the cause.
Area of Science:
- Hematology
- Genetics
- Clinical Diagnostics
Background:
- Hemoglobinopathies are common inherited blood disorders caused by globin gene mutations.
- Conventional methods like electrophoresis and HPLC identify many hemoglobin variants, but DNA analysis is sometimes needed for confirmation.
- Secondary polycythemia can have various causes, including certain hemoglobinopathies.
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