Brachydactyly and short stature in a kindred with early-onset parkinsonism

Am J Med Genet A. 2004 Sep 15;130A(1):102-4. doi: 10.1002/ajmg.a.30021.

Abstract

In a Dutch kindred we have identified a deletion of the DJ-1 gene, leading to autosomal-recessive parkinsonism. The parkinsonism patients also had short stature and brachydactyly. In the family and a control group from the same community, we used the DJ-1 deletion as a marker for the originally linked PARK7 region and found a significant association with body height (P = 0.005), which suggests a gene in linkage disequilibrium with DJ-1 to be implicated in short stature. Analysis of hand-bone length showed incomplete segregation of the PARK7 region with brachydactyly, such that a gene in PARK7 is unlikely to fully explain the brachydactyly. Since the bone length reduction was more pronounced in the homozygous parkinsonism patients than in their heterozygous relatives, however, the PARK7 region may contain a modifier gene for growth.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Body Height*
  • Case-Control Studies
  • Female
  • Genotype
  • Growth / genetics
  • Hand Deformities / genetics*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Oncogene Proteins / genetics*
  • Parkinsonian Disorders / genetics*
  • Pedigree
  • Phenotype
  • Protein Deglycase DJ-1
  • Signal Transduction
  • Syndrome

Substances

  • Intracellular Signaling Peptides and Proteins
  • Oncogene Proteins
  • PARK7 protein, human
  • Protein Deglycase DJ-1