Epidermolysis bullosa simplex

Cutis

Volumn 70, Issue 1, 2002, Pages 19-21

  Okulicz, Jason F ^a   Kihiczak, Nadia I ^a   Janniger, Camila K ^a  

^a RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLASSIFICATION; EPIDERMOLYSIS BULLOSA SIMPLEX; HUMAN; PATHOLOGY;

EPIDERMOLYSIS BULLOSA SIMPLEX; HUMANS;

EID: 0036633144     PISSN: 00114162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. Fine JD, Johnson LB, Suchindron C, et al. The epidemiology of inherited EB: findings within American, Canadian, and European study populations. In: Fine JD, Bauer EA, McGuire J, et al, eds. Epidermolysis Bullosa: Findings of the National Epidermolysis Bullosa Registry. Baltimore, Md: Johns Hopkins University Press; 1999:100-113.
2. Muller FB, Kuster W, Bruckner-Tuderman L, et al. Novel K5 and K14 mutations in German patients with the Weber-Cockayne variant of epidermolysis bullosa simplex. J Invest Dermatol. 1998;111:900-902.
3. Fuchs E. Genetic skin disorders of keratin. J Invest Dermatol. 1992;99:671-674.
4. Combemale P, Kanitakis J. Epidermolysis bullosa simplex with mottled pigmentation: case report and review of the literature. Dermatology. 1994;189:173-178.
5. Shemanko CS, Mellerio JE, Tidman MJ, et al. Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14). J Invest Dermatol. 1998;111:893-895.
6. Kunz M, Rouan F, Pulkkinen L, et al. Mutation reports: epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin gene. J Invest Dermatol. 2000;114:376-380.
7. Horn HM, Tidman MJ. The clinical spectrum of epidermolysis bullosa simplex. Br J Dermatol. 2000;142:468-472.
8. Köbner H. Hereditare anlage zur blasenbildung (epidermolysis bullosa hereditaria). Dtsch Med Wochenschr. 1886;21-22.
9. Smack DP, Korge BP, James WD. Keratin and keratinization. J Am Acad Dermatol. 1994;30:85-102.
10. Fine JD, Eady RA, Bauer EA, et al. Revised classification system for inherited epidermolysis bullosa: report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa. J Am Acad Dermatol. 2000;42:1051-1066.
11. Retief CR, Malkinson FD, Pearson RW. Two familial cases of epidermolysis bullosa simplex successfully treated with tetracycline. Arch Dermatol. 1999;135:997-998.
12. Fuchs E, Coulombe P, Cheng J, et al. Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis. J Invest Dermotol. 1994;103(suppl 5):25S-30S.