Hereditary elliptocytosis: A novel mutation in the SPTA1 gene and diagnosis after a stroke in paediatric patients. A two-case report.

Noelia Moreno-ToroAna Gámez BelmonteSofía Alperi GarcíaÁngel Morillas MingoranceMaría José Ortega AcostaEmilia Urrutia MaldonadoMónica Bernal SánchezIrene Peláez Pleguezuelos

Published in: Pediatric blood & cancer (2023)

Keyphrases

case report
end stage renal disease
ejection fraction
newly diagnosed
chronic kidney disease
intensive care unit
peritoneal dialysis
atrial fibrillation
prognostic factors
patient reported outcomes
gene expression
cerebral ischemia
patient reported