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Cutaneous mosaicism, in KRT 1 pI 479T patient, caused by the somatic loss of the wild‐type allele, leads to the increase in local severity of the disease
Author(s) -
Palombo R.,
Giannella E.,
Didona B.,
AnnicchiaricoPetruzzelli M.,
Melino G.,
Terrii A.
Publication year - 2016
Publication title -
journal of the european academy of dermatology and venereology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 107
eISSN - 1468-3083
pISSN - 0926-9959
DOI - 10.1111/jdv.13153
Subject(s) - palmoplantar keratoderma , epidermolytic hyperkeratosis , medicine , dermatology , ichthyosis , allele , hyperkeratosis , keratoderma , genetics , phenotype , genodermatosis , gene , biology
Background Epidermolytic ichthyosis ( BCIE , OMIM 113800), is an autosomal dominant disorder of the skin caused by mutations in keratin genes KRT 1 and KRT 10. We present two sporadic patients showing a mild diffuse ichthyosis with palmoplantar keratoderma. Interestingly, one of them shows a significant hyperkeratosis of palms and soles similar to those present in the Meleda disease ( OMIM 248300). Objective In this paper we would clarify the genetic difference between the two patients, giving rise to the different phenotype. Methods Clinical evaluation, followed by histological and molecular analysis has been established for these patients. Results We demonstrated the presence of a genetic cutaneous mosaicism. Both patients carry the KRT 1 pI 479T substitution, but in the palmoplantar areas of one of them, only the mutated allele is expressed (hemizygous). This leads to highlight a new type of cutaneous mosaic, the palmoplantar mosaicism.