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Eliptocitosis de tipo hereditario
Es un trastorno que se transmite de padres a hijos, en el cual los glóbulos rojos sanguíneos tienen una forma anormal.
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La eliptocitosis afecta aproximadamente a 1 de cada 2,500 personas de origen europeo del norte. Es más común en personas de ascendencia africana y mediterránea. Existe una mayor probabilidad de desarrollar esta enfermedad si alguien en la familia la ha padecido.
Golan DE. Hemolytic anemias: red cell membrane and metabolic defects. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 165.
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