Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/50966
Title: One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia
Authors: Abrahao, Agessandro [UNIFESP]
Neto, Osorio Abath
Kok, Fernando
Zanoteli, Edmar
Santos, Bibiana
Vieira de Rezende Pinto, Wladimir Bocca [UNIFESP]
Povoas Barsottini, Orlando Graziani [UNIFESP]
Bulle Oliveira, Acary Souza [UNIFESP]
Pedroso, Jose Luiz [UNIFESP]
Keywords: Inclusion body myopathy
Frontotemporal dementia
Amyotrophic lateral sclerosis
VCP
Valosin-containing protein
Issue Date: 2016
Publisher: Elsevier Science Bv
Citation: Journal Of The Neurological Sciences. Amsterdam, v. 368, p. 352-358, 2016.
Abstract: Background: VCP (valosin-containing protein gene) variants have been associated with peripheral and central neurodegenerative processes, including inclusion body myopathy (IBM), Paget disease of bone (PDB), frontotemporal dementia (FTD), and familial amyotrophic lateral sclerosis (ALS) type 14. The combination of IBM, PDB (IBMPFD1) can presented in one individual. However, the association of IBMPFD1 and ALS in the same family is rare. Methods: We reported three individuals from a Brazilian kindred with intrafamilial phenotype variability. Whole exome sequencing (WES) of the proband was performed and revealed a novel VCP variant. VCP Sanger sequencing was performed in the proband and his family members to confirm WES finding and segregation. We performed a systematic review of the literature regarding the genotypic-phenotypic VCP correlations. Results: Each individual presented with either myopathy with rimmed vacuoles, ALS, or FTD. There was no PDB. WES of the proband identified the heterozygous variant c.271A> T (p.Asn91Tyr) in the exon 3 of VCP. Sanger sequencing confirmed the segregation of this variant in an autosomal-dominant pattern. Conclusion: This study expands the genotypic spectrum of the missense mutations of the VCP gene with a novel p.Asn9lTyr variant found in a Brazilian family presenting with the unusual intrafamiliar association of myopathy with rimmed vacuoles, ALS and FTD. (C) 2016 Elsevier B.V. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/50966
ISSN: 0022-510X
Other Identifiers: http://dx.doi.org/10.1016/j.jns.2016.07.048
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