Multimodal imaging in a patient with Prader–Willi syndrome

BACKGROUND: Prader–Willi syndrome (PWS) is a genetic disease caused by loss of expression of the paternally inherited copy of several genes on the long arm of chromosome 15. Ophthalmic manifestations of PWS include strabismus, amblyopia, nystagmus, hypopigmentation of the iris and choroid, diabetic...

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Detalles Bibliográficos
Autores principales: Hamid, Mohamed A., Mehta, Mitul C., Kuppermann, Baruch D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267888/
https://www.ncbi.nlm.nih.gov/pubmed/30519487
http://dx.doi.org/10.1186/s40942-018-0147-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267888/
https://www.ncbi.nlm.nih.gov/pubmed/30519487
http://dx.doi.org/10.1186/s40942-018-0147-6

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