Esferocitosis hereditaria en neonatos y su fisiopatología: un enfoque molecular

Maria Clara Vargas Zuluaga (Autor estudiante de pregrado)

Producción científica: Contribución a una publicación especializadaArtículo

Resumen

Hereditary spherocytosis is a cause of hemolytic anemia that commonly affects neonates and infants; where hemolysis occurs due to the spheroidal shape, rigidity and fragility of erythrocytes in peripheral blood. These morphological changes are generated by genetic, protein and external factors to the erythrocyte membrane, which translates into the presence of clinical manifestations of the disease, which if it does not receive a timely diagnosis and early treatment can be responsible for mild to severe complications and even death.
Idioma originalEspañol (Colombia)
Páginas53-59
Volumen9
N.º4
Publicación especializadaSalutem Scientia Spiritus
EstadoPublicada - 2023
Publicado de forma externa

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