Reporte de un probable caso de Hemoglobina S / Talasemia Beta / Report of a probable case of Hemoglobin S / Beta Thalassemia
Rev. méd. hered
;
15(3): 173-178, jul.-sept. 2004. ilus
Article
in Spanish
| LILACS, LIPECS
| ID: lil-409505
ABSTRACT
We report the case of a patient with Hemoglobin S / Thalassemia. It is feasible to recognize this infrequent disease by its clinical presentation and the aid of clinical laboratory. On this patient, the diagnosis was established based on the clinical findings, hematological evaluation (with careful observation of the red cell morphology and reticulocyte count) and electrophoretic analysis of hemoglobin. We discusse the physiopathology, clinical manifestations, treatment and alternative of prevention of this disease.
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Index:
LILACS (Americas)
Main subject:
Hemoglobin, Sickle
/
Beta-Thalassemia
Limits:
Child
/
Female
/
Humans
Language:
Spanish
Journal:
Rev. méd. hered
Year:
2004
Type:
Article
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