Ollier disease

Enchondromatosis is a rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.

Blurred vision

Lack of sharpness of vision resulting in the inability to see fine detail.


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PMID (PMCID)
18414790
 MALE
Cerebellar anaplastic astrocytoma in a teenager with Ollier Disease.
Walid MS, Troup EC.
J Neurooncol. 2008;89(1):59-62.
A 14-year-old, Caucasian male with Ollier Disease presented with a history of headaches, vomiting, blurred vision, and unsteady gait.