Abstract.
We report a 20-year-old woman who had an attack of acute intermittent porphyria with seizures, hallucinations, autonomic and somatic neuropathy. T2-weighted MRI revealed multiple lesions which were no longer visible 3 months later. We suggest a similar mechanism to posterior reversible encephalopathy underlying cerebral symptoms in porphyria.
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Çelik, .M., Forta, .H., Dalkılıç, T. et al. MRI reveals reversible lesions resembling posterior reversible encephalopathy in porphyria. Neuroradiology 44, 839–841 (2002). https://doi.org/10.1007/s00234-002-0823-x
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DOI: https://doi.org/10.1007/s00234-002-0823-x