Craniofacial and dentoalveolar morphology in individuals with Prader–Willi syndrome: a case-control study

BACKGROUND: Prader–Willi syndrome (PWS) is a complex multisystem genetic disorder with distinct genetic and clinical features. Among other clinical symptoms, PWS is characterized by severe infantile hypotonia with feeding problems, childhood onset hyperphagia, obesity, scoliosis, short stature combi...

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Detalles Bibliográficos
Autores principales: Vasconcelos, Gisela, Stenehjem, Jo S., Axelsson, Stefan, Saeves, Ronnaug
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864885/
https://www.ncbi.nlm.nih.gov/pubmed/35193626
http://dx.doi.org/10.1186/s13023-022-02222-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864885/
https://www.ncbi.nlm.nih.gov/pubmed/35193626
http://dx.doi.org/10.1186/s13023-022-02222-y

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