Ontology highlight
ABSTRACT:
SUBMITTER: Terrinoni A
PROVIDER: S-EPMC5918167 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature
Terrinoni Alessandro A Didona Biagio B Caporali Sabrina S Chillemi Giovanni G Lo Surdo Alessandro A Paradisi Mauro M Annichiarico-Petruzzelli Margherita M Candi Eleonora E Bernardini Sergio S Melino Gerry G
PloS one 20180424 4
Ichthyosis Hystrix of Curth-Macklin (IH-CM) is a rare manifestation of epidermolytic ichthyosis (EI) that is characterised by generalised spiky or verrucous hyperkeratosis. The disorder is further distinguished by the presence of binucleated cells in the affected skin, whereas epidermolysis and clumping of tonofilaments, as seen in EI, are absent. While IH-CM is associated with mutations in the keratin 1 (KRT1) gene, reports to date have indicated that mutations in the KRT1 gene result in an abe ...[more]