Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
Author:
Affiliation:
1. Department of Dermatology, Allergology and Venerology; Medical University of Gdansk; Gdansk Poland
2. Dermatology Student s Scientific Association, Allergology and Venerology; Medical University of Gdansk; Gdansk Poland
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jdv.14222/fullpdf
Reference10 articles.
1. Monilethrix: a typical case report with microscopic and dermatoscopic findings;Oliveira;An Bras Dermatol,2015
2. Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype;Korge;J Invest Dermatol,1999
3. Two different mutations in the same codon of a type II hair keratin (hHb6) in patients with monilethrix;Pearce;J Invest Dermatol,1999
4. Monilethrix: a new family with the novel mutation in KRT81 gene;Ferrando;Int J Trichol,2012
5. A novel missense mutation, A118E, in the helix initiation motif of the type II hair cortex keratin hHb6, causing monilethrix;Winter;Hum Hered,2000
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