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Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
Homozygous sickle cell anemia and secondary complications: a case study
Christopher J Yontz1, Kathy V Waller
1The Ohio State University, 535 Atwell Hall, 453 W. 10th Avenue, Columbus, OH 43210, USA. yontz.17@buckeyemail.osu.edu
Abstract:
A 26-year-old African-American male presented with chest and back pain, fatigue and a history of the following: homozygous sickle cell anemia, pain crises, stroke, hip replacement following avascular necrosis of the femoral head, priapism, chronic transfusions, iron overload, hypertension, migraine headaches, port infections, depression and type II diabetes.
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