Glomerulonefritis fibrilar extrarrenal como nueva etiología de enfermedad hepática avanzada
Carlos Alventosa Mateu, Ana Vilar Gimeno(Sociedad Española de Nefrología), Irene Pérez Álvarez, Javier Carbonell Zamorano(Hospital General Universitario De Valencia), Inmaculada Castelló Miralles, Mercedes Latorre Sánchez, Juan José Urquijo Ponce, Encarnación Martínez Leandro(Hospital General Universitario De Valencia), Liria Terrádez Mas(Hospital Clínico Universitario de Valencia), M. Diago
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Abstract
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.
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