PMID: 9655320Jul 9, 1998Paper

Keratitis, ichthyosis, and deafness (KID) syndrome in half sibs

Pediatric Dermatology
I Koné-PautP Berbis

Abstract

The keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of the ectoderm characterized by diffuse hyperkeratotic erythroderma, keratitis with neovascularization of the cornea, and severe neurosensory hearing loss. A familial occurrence of this syndrome has been mentioned in four reports including three of vertical transmission and one of two affected sisters born from consanguineous, unaffected parents. We report for the first time a familial case of KID syndrome in two half siblings born to the same unaffected mother. This new observation allows us to propose various hypotheses about its mode of inheritance.

Citations

Feb 15, 2005·Clinics in Dermatology·Gabriele Richard
Apr 7, 1999·Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie·N AndréP Berbis
May 25, 1999·Pediatric Dermatology·L RestanoG Tadini
May 3, 2000·Pediatric Dermatology·H C NousariJ L Pinto
Apr 13, 2005·Acta Dermato-venereologica·Anette BygumMarkus M Nöthen
Mar 13, 2002·The Laryngoscope·Yvonne M Szymko-BennettAndrew J Griffith
Jan 27, 2016·International Journal of Pediatric Otorhinolaryngology·T G MarkovaG A Tavartkiladze
Feb 7, 2013·Journal of the American Academy of Dermatology·Kathleen CoggshallKanade Shinkai
Mar 24, 2010·Biochemical and Biophysical Research Communications·Alessandro TerrinoniGerry Melino
Mar 17, 2010·Biochemical and Biophysical Research Communications·Alessandro TerrinoniGerry Melino
Oct 16, 2004·The Journal of Investigative Dermatology·Gabriele RichardAlfons Krol
Mar 29, 2002·The Journal of Investigative Dermatology·Maurice A M van SteenselPeter M Steijlen
Mar 4, 2008·International Journal of Pediatric Otorhinolaryngology·Sharon L CushingBlake C Papsin
Jun 25, 2005·Journal français d'ophtalmologie·R TabetT Hoang-Xuan
Apr 20, 2007·International Journal of Dermatology·Luciana A ConradoNeusa L Dillon
Mar 26, 2002·American Journal of Human Genetics·Gabriele RichardLaura Russell

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