Multimodal ocular imaging in Proteus syndrome

In this report we illustrate the ophthalmologic assessment of two patients affected by Proteus Syndrome (PS), an extremely rare genetic disorder. Case #1 describes a 26 year old male patient followed for multiple ophthalmic anomalies: a limbal dermoid cyst, a unilateral cataract, bilateral nystagmus...

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Detalles Bibliográficos
Autores principales: Salerni, Annabella, Scartozzi, Luca, Piccinni, Fabrizio, Mosca, Luigi, Mattei, Roberta, Leoni, Chiara, Onesimo, Roberta, Zampino, Giuseppe, Rizzo, Stanislao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469497/
https://www.ncbi.nlm.nih.gov/pubmed/36113118
http://dx.doi.org/10.1177/11206721221125852

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469497/
https://www.ncbi.nlm.nih.gov/pubmed/36113118
http://dx.doi.org/10.1177/11206721221125852

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