A novel missense mutation in CYLD in a family with Brooke-Spiegler syndrome

Hu G., Onder M., Gill M., Aksakal B., Oztas M. O., Gurer M., ...More

JOURNAL OF INVESTIGATIVE DERMATOLOGY, vol.121, no.4, pp.732-734, 2003 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 121 Issue: 4
  • Publication Date: 2003
  • Doi Number: 10.1046/j.1523-1747.2003.12514.x
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.732-734
  • Keywords: familial cylindromatosis, turban tumor syndrome, cylindroma, trichoepithelioma, genodermatosis, TUMOR-SUPPRESSOR GENE, MALIGNANT TRANSFORMATION, TURBAN TUMOR, CYLINDROMATOSIS, SKIN, FEATURES, GLAND
  • Gazi University Affiliated: Yes


Brooke-Spiegler syndrome (BSS, familial cylindromatosis or turban tumor syndrome) is an inherited disease characterized by neoplasms of the skin appendages such as cylindroma, trichoepithelioma, and spiradenoma. The disease has been mapped to 16q12-13, and mutations in the CYLD gene have been identified in families with this disorder. Of interest, multiple familial trichoepithelioma (MFT) has been described as a distinct disorder characterized by the familial occurrence of trichoepitheliomas. MFT has been mapped to 9p21; however, to date a candidate gene has not been identified. In this report, we describe a four-generation family with BSS presenting predominantly with trichoepitheliomas (resembling MFT phenotype). We identified a novel missense mutation in the CYLD gene, designated E474G, in the affected individuals of this family. Our findings exemplify clinical heterogeneity within BSS and extend the body of evidence that mutations in CYLD are implicated in this disease. Although not conclusive, these findings suggest that BSS and MFT may represent a single entity.