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Adult-onset neuronal ceroid lipofuscinosis misdiagnosed as autoimmune encephalitis and normal-pressure hydrocephalus: a 10-year case report and literature review

2024-02-06

Abstract excerpt

<h4>Background: </h4> Neuronal ceroid lipofuscinoses (NCLs) are rare, fatal, inherited neurodegenerative disorders characterized by myoclonic epilepsy, cognitive decline, brain atrophy, and retinopathy. The pathogenesis and clinical manifestations of NCL are not well understood and frequently result in misdiagnosis and overtreatment. Case presentation: We present a case of adult-onset NCL (ANCL) that initially pre...

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Literature Corpus work
031ea094-4ad6-5eb8-bc66-4fc82a21863a
DOI
10.21203/rs.3.rs-3924115/v1
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Adult-onset neuronal ceroid lipofuscinosis misdiagnosed as autoimmune encephalitis and normal-pressure hydrocephalus: a 10-year case report and literature reviewDOI 10.21203/rs.3.rs-3924115/v1
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