In vivo structural neuroimaging evaluation of the hypothalamus in Prader-Willi Syndrome sub-genotypes

Abstract Purpose Prader-Willi Syndrome (PWS) is a rare genetic disorder with a heterogeneous phenotype, caused by loss of expression of genes on the paternally inherited chromosome 15q11.2-15q13.3, primarily due to paternal deletion of these genes. PWS with paternal deletion can be categorised into...

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Autors principals:	Marten J. Peters, Esther M. Speksnijder, I. Caroline van Nieuwpoort, Alberto M. Pereira, Madeleine L. Drent, Dirk Jan Stenvers, Chun-Xia Yi
Format:	Artigo
Idioma:	Inglês
Publicat:	Springer 2026-04-01
Col·lecció:	Journal of Rare Diseases
Matèries:	Prader-Willi Syndrome Neuroimaging Magnetic resonance imaging Brain Hypothalamus Cerebellum
Accés en línia:	https://doi.org/10.1007/s44162-026-00173-7
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