Oral manifestations as the main feature of late-onset recessive dystrophic epidermolysis bullosa
Author:
Affiliation:
1. Faculty of Medicine; Department of Dermatology; Medical Center; University of Freiburg; Freiburg im Breisgau Germany
2. Faculty of Medicine; Department of Human Genetics; Medical Center; University of Freiburg; Freiburg im Breisgau Germany
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jdv.14663/fullpdf
Reference7 articles.
1. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification;Fine;J Am Acad Dermatol,2014
2. Research techniques made simple: immunofluorescence antigen mapping in epidermolysis bullosa;Has;J Invest Dermatol,2016
3. Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function;Zimmer;Br J Dermatol,2017
4. Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort;Kern;Br J Dermatol,2009
5. Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes;Varki;J Med Genet,2007
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Lesions of the Oral Cavity;Gnepp's Diagnostic Surgical Pathology of the Head and Neck;2021
2. Endodontic management of a patient with dystrophic epidermolysis bullosa: A case report;Australian Endodontic Journal;2020-12-23
3. Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa;Special Care in Dentistry;2020-11
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