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Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: identification of a recurrent p.P25L mutation in KRT5 in four affected family members.
- Source :
- British Journal of Dermatology; Mar2016, Vol. 174 Issue 3, p633-635, 3p
- Publication Year :
- 2016
-
Abstract
- The article describes the case of epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia in a 28-year-old Japanese man. Topics discussed include asymptomatic reticulate hyper- and hypopigmentation on the trunk and extremities, anomalous polymorphous keratinocytes with dilated intercellular spaces, and p.P25L mutation in KRT5 in all the affected family members.
- Subjects :
- KERATINOCYTES
Subjects
Details
- Language :
- English
- ISSN :
- 00070963
- Volume :
- 174
- Issue :
- 3
- Database :
- Complementary Index
- Journal :
- British Journal of Dermatology
- Publication Type :
- Academic Journal
- Accession number :
- 113901977
- Full Text :
- https://doi.org/10.1111/bjd.14083