Specificity of Early Childhood Hyperphagia Profiles in Neurogenetic Conditions

Hyperphagia is highly penetrant in Prader-Willi syndrome (PWS) and has increasingly been reported in other neurogenetic conditions (NGC). The Hyperphagia Questionnaire (HQ) was completed by caregivers of 4-8-year-olds with PWS (n = 17), Angelman syndrome (AS; n = 22), Williams syndrome (WS; n = 25),...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal on intellectual and developmental disabilities 2024-05, Vol.129 (3), p.175-190
Hauptverfasser: Andrews, Sara M, Panjwani, Anita A, Potter, Sarah Nelson, Hamrick, Lisa R, Wheeler, Anne C, Kelleher, Bridgette L
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!