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Article

Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome.

Genes - 2 Jul 2020

Shepherd Daisy A, Vos Niels, Reid Susan M, Godler David E, Guzys Angela, Moreno-Betancur Margarita, Amor David J

Abstract excerpt

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. This study aimed to investigate growth trajectories in PWS and associations between PWS subtype (deletion vs....

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Identifiers

PMID: 32630716
DOI: 10.3390/genes11070736
PMCID: PMC7397071

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