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An Autopsy Case of Frontotemporal Dementia with Motor Neuron Disease
Article in Korean | WPRIM (Western Pacific) | ID: wpr-133669
Responsible library: WPRO
ABSTRACT
Approximately 15% of patients with frontotemporal dementia (FTD) have co-occurring motor neuron disease (MND). FTD-MND cases have frontotemporal lobar degeneration (FTLD)-transactive response DNA-binding protein (TDP) pathology, which is divided into four subtypes (types A, B, C, and D) based on the morphological appearance, cellular location, and distribution of the abnormal TDP inclusions and dystrophic neurites. We report a patient with FTD-MND whose pathological diagnosis was FTLD-TDP type B. This is the first documented autopsy-confirmed case of FTD-MND in Korea.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Pathology / Autopsy / Neurites / Motor Neuron Disease / Diagnosis / Frontotemporal Lobar Degeneration / Frontotemporal Dementia / Korea / Motor Neurons Type of study: Diagnostic study Limits: Humans Country/Region as subject: Asia Language: Korean Journal: Journal of the Korean Neurological Association Year: 2015 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Pathology / Autopsy / Neurites / Motor Neuron Disease / Diagnosis / Frontotemporal Lobar Degeneration / Frontotemporal Dementia / Korea / Motor Neurons Type of study: Diagnostic study Limits: Humans Country/Region as subject: Asia Language: Korean Journal: Journal of the Korean Neurological Association Year: 2015 Document type: Article
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