Table 1_Rethinking phenylalanine levels in phenylketonuria for optimal neurocognitive development beyond childhood.pdf

Table 1_Rethinking phenylalanine levels in phenylketonuria for optimal neurocognitive development beyond childhood.pdf

Introduction<p>Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism that disrupts neurotransmitter balance. Although early intervention has improved outcomes, neurocognitive challenges persist, particularly during adolescence. Metabolic control guidelines for patients age...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsman: Beatriz Câmara (21570638) (author)
Övriga upphovsmän: Cristina Florindo (284304) (author), Cláudia Bandeira de Lima (21570641) (author), Nélia Correia (21570644) (author), Inês Fernandes (21570647) (author), Manuela Batista (15185435) (author), Ana Gaspar (7131023) (author), Patrícia Janeiro (9562309) (author)
Publicerad: 2025
Ämnen:
Foetal Development and Medicine
adolescent development
cognition
executive function
intelligence tests
phenylketonuria
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk