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Updated: Mar 18, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Unrecognized hemoglobin SE disease as microcytosis
Avery Smith1, Barry Cooper1, Joseph Guileyardo1
1Department of Internal Medicine (Smith), Department of Hematology and Oncology (Cooper), Department of Forensic Pathology (Guileyardo), and Division of Pulmonology and Critical Care (Mora), Baylor University Medical Center at Dallas.
Abstract:
Hemoglobin SE disease was first described during the 1950s as a relatively benign microcytosis, but increasing prevalence has revealed a predisposition towards vasoocclusive sickling. Recognition of SE hemoglobinopathies' potential complications is crucial so medical measures can be utilized to avoid multiorgan injury.
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