Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation

British Journal of Dermatology

Volumn 165, Issue 6, 2011, Pages 1290-1292

  Akasaka, E ^a   Nakano, H ^a   Nakano, A ^b   Toyomaki, Y ^a   Takiyoshi, N ^a   Rokunohe, D ^a   Nishikawa, Y ^a   Korekawa, A ^a   Matsuzaki, Y ^a   Mitsuhashi, Y ^c   Sawamura, D ^a  

^a HIROSAKI UNIVERSITY   (Japan)

^b EST 2 Clinic   (Japan)

^c TOKYO MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

KERATIN; KERATIN 6C; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; FEMALE; GENE; HETEROZYGOTE; HUMAN; HYPERKERATOSIS; JAPANESE; KRT 6C GENE; MALE; PALMOPLANTAR KERATODERMA; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; SYMPTOM;

ADULT; FEMALE; FOOT DERMATOSES; HAND DERMATOSES; HETEROZYGOTE; HUMANS; KERATIN-6; KERATODERMA, PALMOPLANTAR; MALE; MUTATION; PEDIGREE;

EID: 82255164097     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2011.10552.x     Document Type: Article

References (5)

1. Wilson NJ, Messenger AG, Leachman SA, et al. Keratin K6c mutations cause focal palmoplantar keratoderma. J Invest Dermatol 2010; 130: 425-9.
2. McLean WHI, Smith FJD, Cassidy AJ,. Insights into genotype-phenotype correlation in pachyonychia congenita from the Human Intermediate Filament Mutation Database. J Investig Dermatol Symp Proc 2005; 10: 31-6.
3. Leachman SA, Kaspar RL, Fleckman P, et al. Clinical and pathological features of pachyonychia congenita. J Investig Dermatol Symp Proc 2005; 10: 3-17.
4. Szeverenyi I, Cassidy AJ, Chung CW, et al. The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases. Hum Mutat 2008; 29: 351-60. (Pubitemid 351364936)
5. Smith FJ, Liao H, Cassidy AJ, et al. The genetic basis of pachyonychia congenita. J Investig Dermatol Symp Proc 2005; 10: 21-30.