Compound Heterozygous Sickle and Thalassemia Trait: A Case Report.
Article
in En
| IMSEAR
| ID: sea-147171
Sickle cell disease is a type of hemoglobinopathy, which is fairly common in certain parts of the world. We would like to report an interesting case of a child who was labeled as sickle cell anemia but subsequently turned out to be a case of compound heterozygous sickle cell and thalassemia trait.
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IMSEAR
Language:
En
Year:
2011
Type:
Article