A novel mutation of CYLD in a Chinese family with multiple familial trichoepithelioma

J Eur Acad Dermatol Venereol. 2012 Nov;26(11):1420-3. doi: 10.1111/j.1468-3083.2011.04309.x. Epub 2011 Nov 4.

Abstract

Background: Trichoepithelioma is a benign cutaneous tumour that originates from hair follicles and occurs either as a sporadic non-familial or a multiple-familial type. Recently, several mutations in the cylindromatosis (CYLD) gene have been reported in multiple familial trichoepithelioma (MFT).

Objectives: To report a Chinese family of MFT and to explore the genetic mutation.

Methods: A Chinese pedigree of typical MFT was subjected to mutation detection in CYLD. Direct sequencing of all PCR products of the whole coding regions of CYLD gene was performed to identify the mutation.

Results: The c.1178-1179delCA (p.T393fs) mutation was found in CYLD gene in the affected members, but not in the healthy individuals in the family.

Conclusion: Our study found a novel mutation in exon 10 of CYLD gene.

Publication types

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

MeSH terms

  • Adolescent
  • China
  • Female
  • Humans
  • Male
  • Mutation*
  • Neoplastic Syndromes, Hereditary / genetics*
  • Pedigree
  • Polymerase Chain Reaction
  • Skin Neoplasms

Supplementary concepts

  • Familial cylindromatosis