Anemia drepanocítica, manifestaciones clínicas y diagnóstico de laboratorio.

Sickle cell anemia is a group of chronic disorders caused by autosomal recessive disorders in which hemoglobin S (Hb S) is present in red blood cells. This pathology appears by a spontaneous mutation on chromosome 11, in which a glutamic acid is replaced by a valine at position 6 of the globin beta...

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Bibliographic Details
Main Author: Álvaro Tigsi, María Fernanda (author)
Other Authors: Asqui Picuña, Joselyn Aída (author)
Format: bachelorThesis
Language:spa
Published: 2024
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Online Access:http://dspace.unach.edu.ec/handle/51000/12362
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