In vivo neuroimaging evidence of hypothalamic alteration in Prader–Willi syndrome

Prader–Willi syndrome is a genetic neurodevelopmental disorder with an early phenotype characterized by neonatal hypotonia, failure to thrive, and immature genitalia. The onset of hyperphagia in childhood and developmental, physical and neuropsychiatric characteristics indicate atypical brain develo...

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Detalles Bibliográficos
Autores principales: Brown, Stephanie S G, Manning, Katherine E, Fletcher, Paul, Holland, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487704/
https://www.ncbi.nlm.nih.gov/pubmed/36147452
http://dx.doi.org/10.1093/braincomms/fcac229

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487704/
https://www.ncbi.nlm.nih.gov/pubmed/36147452
http://dx.doi.org/10.1093/braincomms/fcac229

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