Early-Onset Parkinsonism: Case Report and Review of the Literature

Pediatr Neurol. 2017 Feb:67:102-106.e1. doi: 10.1016/j.pediatrneurol.2015.06.005. Epub 2015 Oct 23.

Abstract

Background: Early-onset parkinsonism can be caused by PTEN-induced putative kinase 1 (PINK1) gene defects and is usually characterized by an age of onset in the fourth decade of life, slow disease progression, resting tremor, rigidity, bradykinesia, postural instability, and levodopa-induced dyskinesia.

Methods: We evaluated a child with early-onset symptoms and performed a literature review for previously reported examples of children aged 18 years or less with PINK1 gene defects.

Results: We describe a five-year-old boy with autosomal recessive early-onset parkinsonism caused by a homozygous missense mutation in the PINK1 gene. This is the youngest individual yet reported with early-onset parkinsonism.

Conclusion: PINK1-type of early-onset parkinsonism can occur in very young patients, and phenotypic expression of PINK1 mutations may depend on age of onset and ethnicity.

Keywords: Parkinson disease; dystonia; early-onset parkinsonism; movement disorders; parkinsonism; pink1.

Publication types

  • Case Reports
  • Review
  • Video-Audio Media
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Homozygote
  • Humans
  • Male
  • Mutation, Missense
  • Parkinsonian Disorders / diagnosis*
  • Parkinsonian Disorders / drug therapy
  • Parkinsonian Disorders / genetics*
  • Parkinsonian Disorders / physiopathology
  • Protein Kinases / genetics*

Substances

  • Protein Kinases
  • PTEN-induced putative kinase