A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10
J Eur Acad Dermatol Venereol
.
2017 Feb;31(2):e68-e69.
doi: 10.1111/jdv.13729.
Epub 2016 May 26.
Authors
M Kono
1
,
K Fukai
2
,
R Omura
2
,
K Sugawara
2
,
D Tsuruta
2
,
K Sugiura
1
,
M Akiyama
1
Affiliations
1
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
2
Department of Dermatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
PMID:
27225831
DOI:
10.1111/jdv.13729
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child
Female
Humans
Hyperkeratosis, Epidermolytic / genetics
Hyperkeratosis, Epidermolytic / physiopathology*
Keratin-10 / genetics*
Mutation*
Substances
KRT10 protein, human
Keratin-10