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A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration
Authors:Alifiya Kapasi  Jared R. Brosch  Kelly N. Nudelman  Sonal Agrawal  Tatiana M. Foroud  Julie A. Schneider
Affiliation:1. Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, USA;2. Department of Neurology, Indianapolis, Indiana University School of Medicine, Indianapolis, Indiana, USA;3. Indiana Alzheimer Disease Center, Indiana University School of Medicine, Indianapolis, Indiana, USA

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD), Indiana University School of Medicine, Indianapolis, Indiana, USA;4. Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, USA

Department of Pathology, Rush University Medical Center, Chicago, Illinois, USA

Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA

Abstract:
In this case report, we discuss a patient presenting with parkinsonism followed by a non-amnestic dementia with aphasic clinical features, as well as frontal dysexecutive syndrome. There was a family history of dementia with an autopsy diagnosis of “Pick's disease” in the proband's father. Neuroimaging of the patient revealed focal and severe temporal lobe and lesser frontoparietal lobe atrophy. At autopsy, there was severe frontotemporal lobar degeneration. Histologic evaluation revealed an absence of tau or transactivation response DNA-binding protein of 43 kDa (TDP) pathology but rather severe Lewy body deposition in the affected cortices. Genetic phenotyping revealed a novel missense mutation (p.E83Q) in exon 4 of the gene encoding α-synuclein (SNCA). This case study presents a patient with a novel SNCA E83Q mutation associated with widespread Lewy body pathology with prominent severe atrophy of the frontotemporal lobes and corresponding cognitive impairment.
Keywords:case report  dementia  frontotemporal lobar degeneration  Lewy bodies  parkinsonism
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