Superficial Epidermolytic Ichthyosis-Hypertrichosis as a Clue to Diagnosis

Pediatr Dermatol. 2016 Nov;33(6):e346-e348. doi: 10.1111/pde.12955. Epub 2016 Sep 7.

Abstract

Superficial epidermolytic ichthyosis (SEI) is an autosomal dominant disorder caused by a mutation in the keratin 2 gene and clinically characterized by mild hyperkeratosis, superficial blisters and shedding, referred to as the moulting phenomenon. We report a case of SEI in an 18-month-old girl presenting with marked hypertrichosis. Although not invariably present, we believe that hypertrichosis can be an important clue for diagnosis.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Humans
  • Hyperkeratosis, Epidermolytic / complications
  • Hyperkeratosis, Epidermolytic / diagnosis*
  • Hyperkeratosis, Epidermolytic / pathology
  • Hypertrichosis / etiology*
  • Infant