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To validate the recently proposed pediatric severity score (PSS) for sickle cell disease (SCD), we retrospectively assembled clinical data from a cohort of 122 patients with SCD (105 S/S or S/β0‐thal. and 17 S/C) followed up for at least 2 years. Besides age and α‐ and β‐globin genotypes, four new parameters were also tested against the PSS: duration of data assembly, neonatal screening, use of transcranial...
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