RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes

Brain Dev. 2005 Mar;27(2):114-7. doi: 10.1016/j.braindev.2004.02.015.

Abstract

Coffin-Lowry syndrome is an X-linked mental retardation disorder with dysmorphism caused by mutation of the ribosomal S6 kinase (RSK2) gene. Coffin-Lowry syndrome patients can experience unusual drop episodes whereby an abrupt loss of muscle tone and falling down can be induced by sudden, unexpected tactile or auditory stimuli. We detected a C913T (R305X) mutation in a female Coffin-Lowry syndrome patient with drop episodes. All mutations in our patient and those previously reported in patients with drop episodes result in premature truncation of the RSK2 protein in the N-terminal kinase domain or upstream of this domain.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Base Sequence
  • Coffin-Lowry Syndrome / complications
  • Coffin-Lowry Syndrome / genetics*
  • DNA Mutational Analysis
  • Female
  • Genotype
  • Humans
  • Mutation
  • Polymerase Chain Reaction
  • Ribosomal Protein S6 Kinases, 90-kDa / genetics*
  • Syncope / etiology*

Substances

  • Ribosomal Protein S6 Kinases, 90-kDa
  • ribosomal protein S6 kinase, 90kDa, polypeptide 3