Epidermolysis bullosa in a child

CLAO Journal

Volumn 28, Issue 2, 2002, Pages 75-76

  Lazzaro, Douglas R ^a,b,c   Kwon, Ik Son ^a  

^a SUNY DOWNSTATE MEDICAL CENTER   (United States)

^b KINGS COUNTY HOSPITAL CENTER   (United States)

^c NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; EPIDERMOLYSIS BULLOSA; EYE DISEASE; EYE IRRITATION; FEMALE; HUMAN; INTRAOCULAR PRESSURE; NYSTAGMUS; SCHOOL CHILD; CHILD; CORNEA; GENETICS; PATHOLOGY; PATHOPHYSIOLOGY; VISUAL DISORDER;

CHILD; CORNEA; EPIDERMOLYSIS BULLOSA; EYE DISEASES; FEMALE; HUMANS; VISION DISORDERS;

EID: 0036527575     PISSN: 07338902     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Fine JD, Bauer EA, Briggaman RA, et al. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. J Am Acad Dermatol 1991;24:119-35.
2. Fine JD, Johnson LB, Tien H, et al. Estimated incidence and prevalence and lifetable projection of years of life lost by each major epidermolysis bullosa (EB) subtype. J Invest dermatol 1996;106:893.
3. Marinkovich MP. The molecular genetics of basement membrane diseases. Arch Dermatol 1993;129:1557-65.
4. Hintner H, Wolff K. Generalized atrophic benign epidermolysis bullosa. Arch Dermatol 1982;118:375-84.
5. Gil SG, Brown TA, Ryan MC, et al. Junctional Epidermolysis bullosa: Defects in expression of epiligrin/nicein/kalinin and integrin beta 4 that inhibit hemidesmosome formation. J Invest Dermatol 1994;103:31s-38s.
6. Hashimoto I, Schnyder UW, Anton-Lamprecht I. Epidermolysis bullosa hereditaria with junctional blistering in an adult. Dermatologica 1976;152:72-86.