Identification of a Premature Termination Mutation in the Proline-Rich Transmembrane Protein 2 Gene in a Chinese Family with Febrile Seizures

Mol Neurobiol. 2016 Mar;53(2):835-841. doi: 10.1007/s12035-014-9047-4. Epub 2014 Dec 15.

Abstract

Febrile seizures (FS), the most frequent type of seizures in children, occur in neurologically normal infants and children between the ages of 3 months and 5 years with genetic predisposition. The aim of this study was to identify the responsible gene in a four-generation Chinese Han pedigree with autosomal dominant FS. Seven family members (three affected and four unaffected) were enrolled in this study. Exome sequencing was conducted and a duplication mutation c.649dupC (p.R217Pfs*8) in the proline-rich transmembrane protein 2 gene (PRRT2) was identified. The mutation co-segregated with the disorder and was absent in normal controls. To our knowledge, this is the first report of a pedigree with complete penetrance of FS, which is caused by mutation in the PRRT2 gene. FS is a novel phenotype of the c.649dupC (p.R217Pfs*8) mutation. Our discovery broadens the spectrum of genetic causes of FS and the spectrum of phenotypes linked to mutation in the PRRT2 gene.

Keywords: Exome sequencing; Febrile seizures; Genetic counseling; Mutation; PRRT2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Asian People / genetics*
  • Base Sequence
  • Codon, Nonsense / genetics*
  • Exome / genetics
  • Family
  • Female
  • Genetic Predisposition to Disease*
  • Heterozygote
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Molecular Sequence Data
  • Nerve Tissue Proteins / genetics*
  • Pedigree
  • Phenotype
  • Seizures, Febrile / genetics*
  • Young Adult

Substances

  • Codon, Nonsense
  • Membrane Proteins
  • Nerve Tissue Proteins
  • PRRT2 protein, human