A novel homozygous keratin 14 mutation in a patient with autosomal recessive epidermolysis bullosa simplex and squamous cell carcinoma of the tongue
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2009.09614.x/fullpdf
Reference8 articles.
1. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation;Irvine;Br J Dermatol,1999
2. Revised classification system for inherited epidermolysis bullosa: report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa;Fine;J Am Acad Dermatol,2000
3. Epidermolysis bullosa simplex in Israel: clinical and genetic features;Ciubotaru;Arch Dermatol,2003
4. Epidermolysis bullosa simplex with mottled pigmentation resulting from a recurrent mutation in KRT14;Harel;J Invest Dermatol,2006
5. Phenotypes, genotypes and their contribution to understanding keratin function;Porter;Trends Genet,2003
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2. Systemic conditions associated with increased risk to develop oral squamous cell carcinoma: Systematic review and meta‐analysis;Head & Neck;2022-09-16
3. Locally advanced tongue squamous cell carcinoma in epidermolysis simplex bullosa patient: a therapeutic conundrum;The Annals of The Royal College of Surgeons of England;2021-03
4. Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa;Special Care in Dentistry;2020-11
5. Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases;Orphanet Journal of Rare Diseases;2016-08-20
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