Kallin syndrome associated with vitiligo
Author:
Affiliation:
1. Department of Dermatology; Faculty of Medicine; Cairo University; Cairo Egypt
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12463/fullpdf
Reference11 articles.
1. Epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders: a new syndrome;Gamborg Nielsen;Acta Derm Venereol,1985
2. 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
3. The genetic basis of epidermolysis bullosa simplex with mottled pigmentation;Uttam;Proc Natl Acad Sci USA,1996
4. A usual frameshift and delayed termination codon mutation in keratin 5 causes a novel type of epidermolysis bullosa simplex with migratory circinate erythema;Gu;J Invest Dermatol,2003
5. Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease;Betz;Am J Hum Genet,2006
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1. Nail involvement in patients with epidermolysis bullosa: A systematic review;Skin Health and Disease;2022-11-10
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