Superficial epidermolytic ichthyosis: a report of two families

Pediatr Dermatol. 2013 Jul-Aug;30(4):469-72. doi: 10.1111/j.1525-1470.2012.01750.x. Epub 2012 May 21.

Abstract

Superficial epidermolytic ichthyosis (SEI), previously known as ichthyosis bullosa of Siemens, is a rare genetic skin condition, characterized by blisters and hyperkeratosis. It can be easily confused with epidermolytic hyperkeratosis, known now as epidermolytic ichthyosis, and genetic testing can be helpful in differentiating between the two conditions. We describe two children with SEI confirmed by genetic testing, including one with a novel mutation. We also describe other affected family members with SEI.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Diagnosis, Differential
  • Family Health
  • Female
  • Genes, Dominant
  • Heterozygote
  • Humans
  • Hyperkeratosis, Epidermolytic / diagnosis*
  • Hyperkeratosis, Epidermolytic / genetics*
  • Ichthyosis Bullosa of Siemens / diagnosis*
  • Ichthyosis Bullosa of Siemens / genetics*
  • Keratin-2 / genetics*
  • Male

Substances

  • KRT2 protein, human
  • Keratin-2