Expanding Phenotype of VRK1 Mutations in Motor Neuron Disease

J Clin Neuromuscul Dis. 2015 Dec;17(2):69-71. doi: 10.1097/CND.0000000000000096.

Abstract

Objective: In the past decade, hereditary forms of motor neuron disease (spinal muscular atrophy and/or amyotrophic lateral sclerosis) are increasingly identified. As advanced genetic testing is performed, molecular diagnosis can be obtained. Identifying new gene mutations can lead to further understanding of disease.

Methods and results: We report a single case of a patient with early-onset amyotrophic lateral sclerosis, evaluated at University of Texas Health Houston Science Center from 2011-2014. Initial genetic testing did not reveal an etiology in this patient. Through whole-exome sequencing, a VRK1 mutation was identified.

Conclusions and relevance: We identify a possible new cause of hereditary amyotrophic lateral sclerosis, VRK1 mutation. This case report also expands the phenotypic spectrum of this mutation in neurologic diseases.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Computational Biology
  • Genetic Testing
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Male
  • Motor Neuron Disease / genetics*
  • Motor Neuron Disease / pathology
  • Muscle, Skeletal / pathology
  • Mutation / genetics*
  • Phenotype
  • Protein Serine-Threonine Kinases / genetics*

Substances

  • Intracellular Signaling Peptides and Proteins
  • Protein Serine-Threonine Kinases
  • VRK1 protein, human