Ichthyosis follicularis in two girls: an autosomal dominant disorder

Pediatr Dermatol. 1990 Dec;7(4):287-92. doi: 10.1111/j.1525-1470.1990.tb01027.x.

Abstract

Ichthyosis follicularis (IF) is a rare disorder of keratinization that has been described primarily in males and proposed as a possible X-linked disorder. We report two black girls with nonscarring alopecia; photophobia; follicular hyperkeratoses; hyperkeratosis of the extensor aspects of the hands, knees, and elbows; fixed, erythematous, perineal plaques; and angular cheilitis who seem to fit the clinical criteria for IF. One girl also had gingival hypertrophy and a hearing deficit. One child's father had identical symptoms. We propose that these girls may have a variant of IF that is inherited as an autosomal dominant trait.

Publication types

  • Case Reports

MeSH terms

  • Alopecia / diagnosis
  • Child, Preschool
  • Female
  • Humans
  • Ichthyosis, X-Linked / genetics*
  • Ichthyosis, X-Linked / pathology
  • Keratins / metabolism
  • Nail Diseases / pathology

Substances

  • Keratins