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Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia.

Annals of human genetics - 1 Mar 2022

Rizo-delaTorre Lourdes Del Carmen, Herrera-Tirado Isis Mariela, Hernández-Peña Rubiceli, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javier

Abstract excerpt

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency, hereditary spherocytosis (HS), and alpha thalassemia (α-thal) are frequent erythrocyte pathologies with different geographic distributions worldwide. Our aim is to report hematological and molecular findings of G6PD deficient Mexican patients in coinheritance with suggestive hereditary spherocytosis (sHS) and α-thal. METHODS: We studied 78 G6PD...

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PMID: 34844289
DOI: 10.1111/ahg.12451

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