Carlos Alventosa Mateu, Elena Guillen Botaya, Cecilia Albert-Antequera et al.|Journal of Hepatology|2022
Cited by 0Open Access
Hospital General Universitario De Valencia
Publishes on Amyloidosis: Diagnosis, Treatment, Outcomes, COVID-19 Clinical Research Studies, Liver Disease Diagnosis and Treatment. 4 papers and 0 citations.
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Hemoglobin SO-Arab is a rare sickling disorder with a clinical course similar to that of hemoglobin SS. Hemoglobin C-Harlem is another rare condition that produces sickling disorders in affected individuals with a disease course and electrophoretic findings similar to that of hemoglobin SO-Arab. The authors report the case of a 38-year-old African American man with hemoglobin SO-Arab and the challenges that may arise in working up a rare hemoglobinopathy.