Reporte de un probable caso de Hemoglobina S / Talasemia Beta.

Authors

  • John RAMÍREZ CUENTAS
  • Olga LIZAMA OLAYA
  • Josilú MARTÍNEZ LA ROSA
  • Mercy JHONG OLIVERA
  • Eduardo SALAZAR LINDO

DOI:

https://doi.org/10.20453/rmh.v15i3.788

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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Published

2013-01-07

How to Cite

1.
RAMÍREZ CUENTAS J, LIZAMA OLAYA O, MARTÍNEZ LA ROSA J, JHONG OLIVERA M, SALAZAR LINDO E. Reporte de un probable caso de Hemoglobina S / Talasemia Beta. Rev Méd Hered [Internet]. 2013 Jan. 7 [cited 2025 Feb. 4];15(3):173. Available from: http://44.198.254.164/index.php/RMH/article/view/788

Issue

Vol. 15 No. 3 (2004): July - September

Section

BRIEF COMUNICATION

License

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