Expanded C9ORF72 hexanucleotide repeat in depressive pseudodementia.
case_series · Level IV
Where this comes from
- Record sourced from PubMed, PMID 24756204.
- Also identified by DOI 10.1001/jamaneurol.2013.6368 and PMC identifier 4197801.
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Abstract
Expanded hexanucleotide repeats in C9ORF72 are a common genetic cause of frontotemporal dementia and amyotrophic lateral sclerosis. Repeat expansions have also been detected infrequently in other disorders, including Alzheimer disease, dementia with Lewy bodies, and parkinsonian disorders. A consecutive series of 31 cases from the brain bank for neurodegenerative disorders at Mayo Clinic was screened to assess the incidence of the expanded C9ORF72 repeat in cases of depressive pseudodementia. The presence of the hexanucleotide repeat was established using immunohistochemistry with a highly disease-specific antibody (C9RANT), and was further validated in carriers using repeat-primed polymerase chain reaction and Southern blotting. Two individuals harbored the C9ORF72 repeat expansion. Both patients were men with refractory depression. One patient experienced drug-induced parkinsonism and sudden-onset dementia, while the other patient had a more insidious disease course suspected to be Alzheimer disease. This report increases the range of clinicopathologic presentations of C9ORF72 expanded hexanucleotide repeat to include psychiatric disorders such as depressive pseudodementia.
Medical subject headings
- Alzheimer Disease
- Amyotrophic Lateral Sclerosis
- DNA Repeat Expansion
- Depression
- Factitious Disorders
- Frontotemporal Dementia
- Proteins