Craniofacial Fibrous Dysplasia with Orbital Involvement: Two Rare Case Reports and Comprehensive Review

Authors

  • Harikrishnan Marappan
  • Raja Ayakutty Muni

Abstract

Fibrous dysplasia (FD) is a rare, non-heritable bone disorder where normal bone is replaced by fibro-osseous tissue, leading to structural instability and deformities. This report discusses two cases of craniofacial fibrous dysplasia (CFD) with orbital involvement, presenting the clinical findings, diagnostic challenges, and management strategies. Additionally, a comprehensive literature review is provided to offer insights into the pathophysiology, clinical manifestations, and treatment options for this condition.

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Published

2024-12-20

How to Cite

Marappan, H., & Muni, R. A. (2024). Craniofacial Fibrous Dysplasia with Orbital Involvement: Two Rare Case Reports and Comprehensive Review. Archives of Clinical and Medical Case Reports, 8(6), 234–238. Retrieved from https://fortunejournals.org/ojs/index.php/acmcr/article/view/22977