Bullous Dermolysis of the Newborn: Four New Cases and Clinical Review
Author:
Affiliation:
1. University of Michigan Medical School; Ann Arbor Michigan
2. Department of Dermatology; Henry Ford Hospital; Detroit Michigan
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.12230/fullpdf
Reference20 articles.
1. The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on Diagnosis and Classification of EB;Fine;J Am Acad Dermatol,2008
2. Transient bullous dermolysis of the newborn;Hashimoto;Arch Dermatol,1985
3. Intraepidermal type VII collagen: evidence for abnormal intracytoplasmic processing of a major basement membrane protein in rare patients with dominant and possibly localized recessive forms of dystrophic epidermolysis bullosa;Fine;J Am Acad Dermatol,1990
4. Intracytoplasmic retention of type VII collagen and dominant dystrophic epidermolysis bullosa: reversal of defect following cessation of or marked improvement in disease activity;Fine;J Invest Dermatol,1993
5. Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen gene;Christiano;J Invest Dermatol,1997
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