Robustness of Distinctive Facial Features in Prader-Willi Syndrome: A Stereophotogrammetric Analysis and Association with Clinical and Biochemical Markers in Adult Individuals

SIMPLE SUMMARY: Prader-Willi syndrome (PWS) is a rare genetically determined neurodevelopmental disorder usually associated with a peculiar facial appearance. There is poor information concerning the relationships between the facial dysmorphism in PWS and other manifestations of the disease and its...

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Detalles Bibliográficos
Autores principales: Dolci, Claudia, Rigamonti, Antonello E., Cappella, Annalisa, Gibelli, Daniele M., Grugni, Graziano, Caroli, Diana, Sforza, Chiarella, Sartorio, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405094/
https://www.ncbi.nlm.nih.gov/pubmed/36009775
http://dx.doi.org/10.3390/biology11081148

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405094/
https://www.ncbi.nlm.nih.gov/pubmed/36009775
http://dx.doi.org/10.3390/biology11081148

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