Multiple familial trichoepithelioma and familial cylindroma: One cause!

Journal of the European Academy of Dermatology and Venereology

Volumn 22, Issue 11, 2008, Pages 1395-1396

  Oranje, A P ^a,b   Halley, D ^b   Den Hollander, J C ^b   Teepe, R G C ^c   Van De Graaf, R ^b   Van Den Ouweland, A ^b   Wagner, A ^b  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c LEYENBURG HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; CASE REPORT; CHROMOSOME 16; CHROMOSOME 9Q; CHROMOSOME DELETION; CLINICAL FEATURE; CYLD GENE; CYLINDROMA; EXON; FAMILIAL DISEASE; FAMILY HISTORY; GENE; GENE SEQUENCE; GENETIC LINKAGE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INTRON; LETTER; MALE; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SCORING SYSTEM; TRICHOEPITHELIOMA;

ADULT; CARCINOMA, ADENOID CYSTIC; FEMALE; HUMANS; MALE; PEDIGREE; SKIN NEOPLASMS;

EID: 53749100454     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2008.02648.x     Document Type: Letter

References (5)

1. Harada H, Hashimoto K, Ko MSH. The gene for multiple familial trichoepithelioma maps to chromosome 9p21. J Invest Dermatol 1996 107 : 41 43.
2. Zhang X-J, Liang Y-H, He P-P et al. Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma. J Invest Dermatol 2004 122 : 658 664.
3. Zheng G, Hu L, Huang W, Chen K et al. CYLD mutation causes multiple familial trichoepithelioma in three Chinese families. Hum Mutat 2004 23 : 400.
4. Bignell GR, Warren W, Seal S et al. Identification of the familial cylindromatosis tumour-suppressor gene. Nat Genet 2000 25 : 160 165.
5. Oosterkamp HM, Neering H, Nijman SM et al. An evaluation of the efficacy of topical application of salicylic acid for the treatment of familial cylindromatosis. Br J Dermatol 2006 155 : 182 185.