A case report comparing clinical, imaging and neuropsychological assessment findings in twins discordant for the VCP p.R155C mutation

Abhilasha Surampalli, Brian T. Gold, Charles Smith, Rudy J. Castellani, Manaswitha Khare, Hon Yu, Celeste Nguyen, Mary Lan, Marie Wencel, Sharon Wigal, Vince Caiozzo, Virginia Kimonis*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Inclusion body myopathy, Paget disease of bone and/or frontotemporal dementia is an autosomal dominant disease caused by mutations in the Valosin Containing Protein (VCP) gene. We compared clinical findings including MRI images and neuropsychological assessment data in affected and unaffected twin brothers aged 56 years from a family with the p.R155C VCP gene mutation. The affected twin presented with a 10 year history of progressive proximal muscle weakness, difficulty swallowing, gastroesophageal reflux, fecal incontinence, and peripheral neuropathy. Comprehensive neuropsychological testing revealed rapid cognitive decline in the absence of any behavioral changes in a span of 1 year. This case illustrates that frontotemporal dementia related cognitive impairment may precede behavioral changes in VCP disease as compared with predominance of behavioral impairment reported in previous studies. Our findings suggest that there is a need to establish VCP disease specific tools and normative rates of decline to detect pre-clinical cognitive impairment among affected individuals.

Original languageEnglish (US)
Pages (from-to)177-183
Number of pages7
JournalNeuromuscular Disorders
Volume25
Issue number2
DOIs
StatePublished - Feb 1 2015
Externally publishedYes

Keywords

  • Frontotemporal dementia screening
  • Inclusion body myopathy
  • Multisystem proteinopathy
  • Neuropsychological assessment
  • VCP

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Neurology
  • Clinical Neurology
  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'A case report comparing clinical, imaging and neuropsychological assessment findings in twins discordant for the VCP p.R155C mutation'. Together they form a unique fingerprint.

Cite this