Clinical Observations and Treatment Approaches for Scoliosis in Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is recognized as the first example of genomic imprinting, generally due to a de novo paternal 15q11-q13 deletion. PWS is considered the most common genetic cause of marked obesity in humans. Scoliosis, kyphosis, and kyphoscoliosis are commonly seen in children and adolesc...

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Detalles Bibliográficos
Autores principales: van Bosse, Harold J.P., Butler, Merlin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140837/
https://www.ncbi.nlm.nih.gov/pubmed/32121146
http://dx.doi.org/10.3390/genes11030260

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140837/
https://www.ncbi.nlm.nih.gov/pubmed/32121146
http://dx.doi.org/10.3390/genes11030260

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