Interaction of sickle cell trait with hereditary spherocytosis: Splenic infarcts and sequestration

Acta Haematologica

Volumn 109, Issue 1, 2003, Pages 46-49

  Ustun, Celalettin ^a   Kutlar, Ferdane ^a   Holley, Leslie ^a   Seigler, Maree ^a   Burgess, Russell ^a   Kutlar, Abdullah ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

Sickle cell trait; Spherocytosis, hereditary; Splenic infarction; Splenic sequestration

Indexed keywords

GLOBIN; HEMOGLOBIN ALPHA CHAIN;

ADULT; ARTICLE; CASE REPORT; CATION EXCHANGE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; ERYTHROCYTE; HEMOLYSIS; HEREDITARY SPHEROCYTOSIS; HUMAN; HUMAN CELL; ISOELECTRIC FOCUSING; MALE; OSMOTIC FRAGILITY; PRIORITY JOURNAL; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; SICKLE CELL TRAIT; SPLEEN INFARCTION; SPLENOMEGALY; COMORBIDITY; CONGENITAL MALFORMATION; MIDDLE AGED; REVIEW; SICKLE CELL ANEMIA; SPLEEN;

ANEMIA, SICKLE CELL; COMORBIDITY; HEMOLYSIS; HUMANS; MALE; MIDDLE AGED; OSMOTIC FRAGILITY; SPHEROCYTOSIS, HEREDITARY; SPLEEN; SPLENIC INFARCTION; SPLENOMEGALY;

EID: 0037208994     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000067273     Document Type: Article

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