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Correction: Expert opinion of an Italian working group on the assessment of cognitive, psychological, and neurological outcomes in pediatric, adolescent, and adult patients with phenylketonuria

The Original Article was published on 21 December 2022


Correction: Orphanet Journal of Rare Diseases (2022) 17:443 https://doi.org/10.1186/s13023-022-02488-2


Following publication of the original article [1], we have been notified that Table 2, column “Pediatric Patient” should be corrected as per below:


DGS (Forward and Reverse)


Also, reference 40 should be as follows:


40. Quinn J, Georgiadis A, Lewis HB, Jurecki E. Measuring burden of illness in phenylketonuria (PKU): development of the PKU symptom severity and impacts scale as a robust patient-reported outcome. Adv Ther. 2022;39:971–91.

Reference

  1. Manti F, Caviglia S, Cazzorla C, Dicintio A, Pilotto A, Burlina AP. Expert opinion of an Italian working group on the assessment of cognitive, psychological, and neurological outcomes in pediatric, adolescent, and adult patients with phenylketonuria. Orphanet J Rare Dis. 2022;17(1):443. https://doi.org/10.1186/s13023-022-02488-2.

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Correspondence to Alessandro P. Burlina.

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Manti, F., Caviglia, S., Cazzorla, C. et al. Correction: Expert opinion of an Italian working group on the assessment of cognitive, psychological, and neurological outcomes in pediatric, adolescent, and adult patients with phenylketonuria. Orphanet J Rare Dis 18, 44 (2023). https://doi.org/10.1186/s13023-023-02644-2

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  • DOI: https://doi.org/10.1186/s13023-023-02644-2