Cargando…
Epidermolytic Ichthyosis without Keratin 1 or 10 Mutations: A Case Report
In this paper, the authors report a case of an 11-year-old boy with epidermolytic ichthyosis who presented with multiple scattered erosions and typical hyperkeratotic plaques over the face, upper and lower extremities, the trunk, palms and soles. Family history revealed an affected older male siblin...
Autores principales: | Al Raddadi, Ali A., Habibullah, Taha H., Abdelaal, Ahmed M., Felimban, Angie M., Al Raddadi, Hosam A., Satti, Mohamed B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196674/ https://www.ncbi.nlm.nih.gov/pubmed/30787815 http://dx.doi.org/10.4103/1658-631X.220800 |
Ejemplares similares
-
A novel nonsense mutation in keratin 10 causes a familial case of recessive epidermolytic ichthyosis
por: Gutierrez, Jeydith A, et al.
Publicado: (2013) -
Annular epidermolytic ichthyosis: An exceptional mild subtype of epidermolytic ichthyosis without genotype and phenotype correlation
por: Reolid, Alejandra, et al.
Publicado: (2019) -
Epidermolytic Nevus: An Instance of Mosaic Epidermolytic Ichthyosis
por: Adya, Keshavmurthy A., et al.
Publicado: (2020) -
A novel mutation resulting in keratin 1–linked palmoplantar keratoderma with epidermolytic ichthyosis
por: Gray, Taylor, et al.
Publicado: (2020) -
Mosaic epidermolytic ichthyosis - Case report
por: Mendes, Marcela Sena Teixeira, et al.
Publicado: (2013)