Orbital Compression Syndrome In A Ugandan Child With Sickle Cell Disease: A Case Report

Abstract
Orbital compression syndrome is a rare acute complication of sickle cell disease that may impair vision. Assessment by a multidisciplinary team incorporates detailed history and physical examination, fundoscopy, and appropriate imaging to exclude infections or neoplasms. Supportive treatment is adequate unless there is evidence of life-threatening space-occupying lesion warranting surgery.
Description
Keywords
orbital compression syndrome, sickle cell anemia, Uganda
Citation
Olum, R., Nabaggala, C., Mwebe, V. K., Namazzi, R., Munube, D., & Kitaka, S. B. (2021). Orbital compression syndrome in a Ugandan child with sickle cell disease: A case report. Clinical Case Reports, 9(9), e04766.https://doi.org/10.1002/ccr3.4766