KID syndrome associated with features of ichthyosis hystrix

Hossein C. Nousari, Arash Kimyai-Asadi, Jose Luna Pinto

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

Keratitis-ichthyosis-deafness (KID) syndrome is a congenital ectodermal disorder causing erythrokeratoderma, vascularizing keratitis, and neurosensory deafness. Ichthyosis hystrix is a rare cutaneous disease characterized by well-demarcated, spiky, verrucous, linear plaques that is believed to be a clinical and pathologic chimera of two autosomal dominant diseases: epidermal nevus and epidermolytic hyperkeratosis. We present a patient with the classic triad of KID syndrome with clinical and histologic features of ichthyosis hystrix. This case demonstrates that KID syndrome comprises a spectrum of ectodermal disorders which may include diseases such as hystrix ichthyosis and deafness (HID) syndrome.

Original languageEnglish (US)
Pages (from-to)115-117
Number of pages3
JournalPediatric Dermatology
Volume17
Issue number2
DOIs
StatePublished - Sep 9 2000

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Dermatology

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