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...

• מחבר ראשי: Álvaro Tigsi, María Fernanda (author)
• מחברים אחרים: Asqui Picuña, Joselyn Aída (author)
• פורמט: bachelorThesis
• שפה: spa
• יצא לאור: 2024
• נושאים: Anemia drepanocítica; Hematíes; Hemoglobina; Manifestaciones clínicas; Pruebas de laboratorio
• גישה מקוונת: http://dspace.unach.edu.ec/handle/51000/12362