Article
A Case of Ollier's Disease with P53 Mutation Positive and IDH1 (R132H) Negative Multicentric Gliomas.
Neurology India - 1 Jan 2000
Nishtha Y, Maya B, Shetty Safal S, Ganaraj V H, Nupur P, Yasha T C, Netravathi M
Abstract excerpt
Ollier disease is a rare nonhereditary disorder characterized by multiple enchondromas (enchondromatosis). To report a rare case of Ollier disease with gliomas and its mutation analysis. We hereby report a young lady who presented with seizures. She had a past history of multiple bony swellings in the right foot (operated) and swelling over the anterior chest wall for the past 15 years. MRI brain revealed...
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