rss
BMJ Case Reports 2009; doi:10.1136/bcr.06.2009.1994
  • Findings that shed new light on the possible pathogenesis of a disease or an adverse effect

The C20orf133 gene is disrupted in a patient with Kabuki syndrome

  1. Nicole M C Maas1,
  2. Tom Van de Putte2,
  3. Cindy Melotte1,
  4. Annick Francis2,
  5. Constance T R M Schrander-Stumpel3,
  6. Damien Sanlaville4,
  7. David Genevieve4,
  8. Stanislas Lyonnet4,
  9. Boyan Dimitrov1,
  10. Koenraad Devriendt1,
  11. Jean-Pierre Fryns1,
  12. Joris R Vermeesch1
  1. 1
    Centre for Human Genetics, University of Leuven, Leuven, Belgium
  2. 2
    Laboratory of Molecular Biology (Celgen), Division Molecular and Developmental Genetics, Department of Human Genetics, KU Leuven and Department of Molecular and Developmental Genetics (VIB11), Leuven, Belgium
  3. 3
    Department of Clinical Genetics, Academic hospital Maastricht and Research Institute GROW, Maastricht University, Maastricht, The Netherlands
  4. 4
    Department of Genetics, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France
  1. J R Vermeesch, joris.vermeesch{at}med.kuleuven.be
  • Published 30 June 2009

Summary

Kabuki syndrome (KS) is a rare, congenital mental retardation syndrome. The aetiology of KS remains unknown. Four carefully selected patients with KS were screened for chromosomal imbalances using array comparative genomic hybridisation at 1 Mb resolution. In one patient, a 250 kb de novo microdeletion at 20p12.1 was detected, deleting exon 5 of C20orf133. The function of this gene is unknown. In situ hybridisation with the mouse orthologue of C20orf133 showed expression mainly in brain. The de novo nature of the deletion, the expression data and the fact that C20orf133 carries a macro domain, suggesting a role for the gene in chromatin biology, make the gene a likely candidate to cause the phenotype in this patient with KS. Both the finding of different of chromosomal rearrangements in patients with KS features and the absence of C20orf133 mutations in 19 additional patients with KS suggest that KS is genetically heterogeneous.

Footnotes

  • Competing interests: none.

Register for free content

The full text of all Editor's Choice articles and summaries of every article are free without registration

The full text of Images in ... articles are free to registered users

Only fellows can access the full text of case reports (apart from Editor's Choice) - become a fellow today, or encourage your institution to, so that together we can grow and develop this resource

Don't forget to sign up for content alerts so you keep up to date with all the case reports as they are published, and let us know what you think by commenting on the Editor's blog

Navigate This Article