Clinical and molecular characteristics of Cardio-facio-cutaneous syndrome in Hong Kong Chinese

H. M. Luk, I. F.M. Lo, Y. Aoki, T. M.F. Tong, D. H.C. Chan, S. T.S. Lam

Research output: Contribution to journalArticlepeer-review

Abstract

Cardio-facio-cutaneous (CFC) syndrome is a rare disorder of RASopathy that is caused by dysregulation of the RAS/MAPK signaling pathway. Germline mutations of BRAF, MEK1, MEK2 and KRAS genes account for 70-90% of the cases. We have performed mutational analysis for the clinically diagnosed CFC patients under the care of Clinical Genetics Service, Department of Health, Hong Kong Special Administrative Region between 2000 to 2011. Totally 7 unrelated clinically diagnosed Chinese CFC patients were studied. Mutations have been identified in 6 (85.7%) of our patients, including 5 (71.4%) BRAF mutations and 1 (14.2%) MEK2 mutation. Their clinical features were summarised. It can be concluded that the pattern of molecular defects and clinical characteristics of Chinese CFC patients are comparable with other populations without ethnic-specific difference.

Original languageEnglish
Pages (from-to)31-36
Number of pages6
JournalHong Kong Journal of Paediatrics
Volume18
Issue number1
Publication statusPublished - 2013

Keywords

  • BRAF
  • Cardio-facio-cutaneous syndrome
  • Chinese
  • MEK1/2

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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