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pubmed-article:3368073pubmed:abstractTextWe studied four patients with a focal epilepsy and bilateral occipital corticosubcortical calcifications without any sign of phakomatosis. The clinical course of the disease was similar in all the patients and evolved from a benign onset to a severe encephalopathy with progressive mental impairment. The question of whether these patients have an incomplete and atypical form of Sturge-Weber syndrome or a previously undescribed disorder is addressed.lld:pubmed
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pubmed-article:3368073pubmed:articleTitleEpilepsy with bilateral occipital calcifications: a benign onset with progressive severity.lld:pubmed
pubmed-article:3368073pubmed:affiliationDepartment of Child Neurology, University of Bologna Medical School, Italy.lld:pubmed
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