Isolated Unilateral Orbital Compression Syndrome in A 19-Year-Old Male With Homozygous Sickle Cell Disease

This study aimed to report a rare case of a rapidly progressive isolated unilateral orbital compression syndrome in a male with homozygous sickle cell disease, who presented with proptosis and optic nerve dysfunction. He neither had long bone pain crisis nor fever at the time of presentation that wa...

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Detalles Bibliográficos
Autores principales: Almukhtar, Fatema M, Aljufairi, Fatema M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Ophthalmology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575328/
https://www.ncbi.nlm.nih.gov/pubmed/34765338
http://dx.doi.org/10.7759/cureus.18545

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575328/
https://www.ncbi.nlm.nih.gov/pubmed/34765338
http://dx.doi.org/10.7759/cureus.18545

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