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Hemoglobin SO-Arab and α-Thalassemia Diagnosed in an Adult: A Case-Based Review of the Hemoglobinopathies.
MedLine Citation:
PMID:  23221516     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
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.
Authors:
George Zacharia; Genevieve F Maronge; Frederick W Brazda; Brian C Boulmay
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-12-5
Journal Detail:
Title:  The American journal of the medical sciences     Volume:  -     ISSN:  1538-2990     ISO Abbreviation:  Am. J. Med. Sci.     Publication Date:  2012 Dec 
Date Detail:
Created Date:  2012-12-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0370506     Medline TA:  Am J Med Sci     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Departments of Internal Medicine (GZ), Section of Hematology & Oncology (GFM, BCB), and Pathology (FWB), Louisiana State University Health Sciences Center, New Orleans, Louisiana.
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