Literature DB >> 23596077

Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis.

Ashley Cannon1, Shinsuke Fujioka, Nicola J Rutherford, Tanis J Ferman, Daniel F Broderick, Kevin B Boylan, Neill R Graff-Radford, Ryan J Uitti, Rosa Rademakers, Zbigniew K Wszolek, Dennis W Dickson.   

Abstract

OBJECTIVE: We examined the clinical and pathologic phenotypes of GRN mutation carriers with the pathogenic A9D (g.26C>A) missense mutation.
METHODS: Three patients with GRN A9D mutations were evaluated clinically and came to autopsy with subsequent neuropathologic examination.
RESULTS: The clinical diagnoses of patients with GRN A9D mutations were amyotrophic lateral sclerosis, atypical extrapyramidal disorder, and behavioral variant frontotemporal dementia. Immunohistochemistry for TAR DNA-binding protein 43 (TDP-43) revealed variability in morphology and distribution of pathology. One patient had notable involvement of motor neurons in the spinal cord as well as type B TDP-43, whereas 2 other patients had type A TDP-43.
CONCLUSIONS: The clinical presentation of the GRN A9D missense mutation is not restricted to behavioral variant frontotemporal dementia and may include aphasia, extrapyramidal features, and, notably, amyotrophic lateral sclerosis.

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Year:  2013        PMID: 23596077      PMCID: PMC3719429          DOI: 10.1212/WNL.0b013e3182919059

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  20 in total

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