Exclusion of RNX as a major gene in congenital central hypoventilation syndrome (CCHS, Ondine's curse)

Am J Med Genet A. 2003 Feb 15;117A(1):18-20. doi: 10.1002/ajmg.a.10934.

Abstract

Congenital central hypoventilation syndrome (CCHS) is a rare condition for which segregation analyses have suggested genetic factors. The respiratory phenotype of Rnx knock-out mice together with the Rnx expression at the brainstem level prompted us to consider the RNX gene as a candidate for CCHS in human. The screening of the RNX gene in a series of 25 patients with CCHS did not reveal any significant nucleotide variation. We therefore conclude that RNX is not a major gene for CCHS in human.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA / chemistry
  • DNA / genetics
  • DNA Mutational Analysis
  • Female
  • Genetic Predisposition to Disease / genetics
  • Homeodomain Proteins / genetics*
  • Humans
  • Male
  • Oncogene Proteins / genetics*
  • Polymorphism, Single-Stranded Conformational
  • Proto-Oncogene Proteins
  • Sleep Apnea, Central / congenital
  • Sleep Apnea, Central / genetics*
  • Syndrome

Substances

  • Homeodomain Proteins
  • Oncogene Proteins
  • Proto-Oncogene Proteins
  • TLX3 protein, human
  • TLX1 protein, human
  • DNA