Growth Trajectories in Genetic Subtypes of Prader–Willi Syndrome

Growth Trajectories in Genetic Subtypes of Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the paternal copy of chromosome 15q11-13. The main molecular subtypes of PWS are the deletion of 15q11-13 and non-deletion, and differences in neurobehavioral phenotype are recognized between the subtypes. Th...

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Bibliographic Details
Main Authors: Daisy A. Shepherd, Niels Vos, Susan M. Reid, David E. Godler, Angela Guzys, Margarita Moreno-Betancur, David J. Amor
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Genes
Subjects:
Prader–Willi syndrome
weight
obesity
BMI
pediatric
linear mixed models
Online Access:https://www.mdpi.com/2073-4425/11/7/736

Internet

https://www.mdpi.com/2073-4425/11/7/736

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