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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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| Veröffentlicht in: | Int J Retina Vitreous |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6267888/ https://ncbi.nlm.nih.gov/pubmed/30519487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40942-018-0147-6 |
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