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

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.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Koné-Paut I,Hesse S,Palix C,Rey R,Rémédiani K,Garnier JM,Berbis P

doi

10.1046/j.1525-1470.1998.1998015219.x

subject

Has Abstract

pub_date

1998-05-01 00:00:00

pages

219-21

issue

3

eissn

0736-8046

issn

1525-1470

journal_volume

15

pub_type

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