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A Case of autoimmune hemolytic anemia and beta thalassemia,minor ; in acutehemolytic crisis in a 6-year-old boy "gone too soon" a case report / Liana Aira Quibael.

By: Language: English Publication details: Fairview, Quezon City Department of Child Health, FEU-NRMF, 2017Description: illustrations; (in folder)Content type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
LOC classification:
  • CH20170003
Summary: ABSTRACT: This case report aims to discuss a 6 year old male with both hereditary and acquired hemolytic anemia. The approach in diagnosing hemolytic anemia involves: clinical manifestations suggesting hemolytic disease and laboratory demonstration of the presence of a hemolytic anemia.Hemolytic Anemiais due to increase in red blood cell destruction. It can be classified as either hereditary or acquired. Treatment includes addressing the primary cause and specifically blood transfusion and steroids.
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Includes appendices and bibliographical references.

ABSTRACT: This case report aims to discuss a 6 year old male with both hereditary and acquired hemolytic anemia. The approach in diagnosing hemolytic anemia involves: clinical manifestations suggesting hemolytic disease and laboratory demonstration of the presence of a hemolytic anemia.Hemolytic Anemiais due to increase in red blood cell destruction. It can be classified as either hereditary or acquired. Treatment includes addressing the primary cause and specifically blood transfusion and steroids.

Research - Department of Child Health

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