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- W2325101314 abstract "Lipoid Proteinozis (LP) known as Urbach-Wiethe disease is a rare autosomal recessive inherited genodermatozis. Patients usually present with hoarseness and skin-mucosa abnormalities. Lipoid Proteinozis involves the central nervous system (CNS) rarely. The essential imaging finding in LP is appearance of atypical intracranial calcifications, mostly occurring in the medial temporal lobes. Herein we report a rare case presenting with seizure accompanied computed tomography (CT), magnetic resonance imaging (MRI) findings and also with pathological confirmation." @default.
- W2325101314 created "2016-06-24" @default.
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- W2325101314 date "2016-03-21" @default.
- W2325101314 modified "2023-09-23" @default.
- W2325101314 title "A Rare Cause of Seizure; Lipoid Proteinozis (Urbach-Wiethe disease): A Case Report" @default.
- W2325101314 doi "https://doi.org/10.16899/ctd.45513" @default.
- W2325101314 hasPublicationYear "2016" @default.
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