Age Distribution, Comorbidities and Risk Factors for Thrombosis in Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is an imprinting disorder caused by lack of expression of the paternally inherited 15q11.2–q13 chromosome region. The risk of death from obesity-related complications can worsen with age, but survival trends are improving. Comorbidities and their complications such as thr...

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Detalles Bibliográficos
Autores principales: Butler, Merlin G., Oyetunji, Aderonke, Manzardo, Ann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017326/
https://www.ncbi.nlm.nih.gov/pubmed/31936105
http://dx.doi.org/10.3390/genes11010067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017326/
https://www.ncbi.nlm.nih.gov/pubmed/31936105
http://dx.doi.org/10.3390/genes11010067

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