Sickle-cell disease, hemophilia, and hematology

Primary hematologic disorders and the hematologic problems associated with systemic rheumatologic disease have widespread and significant implications for the clinical management of rheumatic disease. This article reviews recently published information on the epidemiology, pathophysiology, and manag...

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Bibliographic Details
Published inCurrent opinion in rheumatology Vol. 5; no. 1; p. 95
Main Author Tozman, E C
Format Journal Article
LanguageEnglish
Published United States 01.01.1993
Subjects
Anemia, Sickle Cell - epidemiology
Anemia, Sickle Cell - physiopathology
Anemia, Sickle Cell - therapy
Hematologic Diseases - epidemiology
Hematologic Diseases - physiopathology
Hematologic Diseases - therapy
Hemophilia A - epidemiology
Hemophilia A - physiopathology
Hemophilia A - therapy
Humans
Rheumatic Diseases - complications
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Summary:Primary hematologic disorders and the hematologic problems associated with systemic rheumatologic disease have widespread and significant implications for the clinical management of rheumatic disease. This article reviews recently published information on the epidemiology, pathophysiology, and management of hemoglobinopathies, hemophilia, and other hematologic pathologies associated with significant rheumatologic manifestations.
ISSN:1040-8711
DOI:10.1097/00002281-199305010-00015