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  Vol. 123 No. 6, June 1987 TABLE OF CONTENTS
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Keratitis, Ichthyosis, and Deafness (KID) Syndrome

Vertical Transmission and Death From Multiple Squamous Cell Carcinomas

Jean Jacques Grob, MD; Annie Breton, MD; Jean Louis Bonafe, MD; Michéle Sauvan-Ferdani, MD; Jean Jacques Bonerandi, MD

Arch Dermatol. 1987;123(6):777-782.


Abstract

• A father and daughter had typical clinical features of the keratitis, ichthyosis, and deafness (KID) syndrome, as described by Skinner et al in 1981. To our knowledge, ours is the first observation of a vertical transmission of this syndrome. The mechanism of inheritance is uncertain. These two patients as well as the 26 previously described exhibited a typical hyperkeratotic eruption, which should not be confused with ichthyosis. The characteristic features are diffuse hyperkeratosis, keratotic plaques, reticulated hyperkeratosis on the face, peribuccal grooves, and heavy-grain leatherlike keratoderma. The occurrence of multiple squamous cell carcinomas underlines the seriousness of this congenital ectodermal defect. Etretinate can relieve the lesions without actually improving the chances of survival.

(Arch Dermatol 1987;123:777-782)



Author Affiliations

From the Dermatovenereology Service, Ste Marguerite Hospital, Marseille, France (Drs Grob, Breton, Sauvan-Ferdani, and Bonerandi); and the Dermatology Service, Rangueil Hospital, Toulouse, France (Dr Bonafe).


Footnotes

Accepted for publication Oct 15, 1986.

Read before the Société Française de Dermatologie, Jan 9,1985.

Reprints not available.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Linkage of an American Pedigree With Palmoplantar Keratoderma and Malignancy (Palmoplantar Ectodermal Dysplasia Type III) to 17q24: Literature Survey and Proposed Updated Classification of the Keratodermas
Stevens et al.
Arch Dermatol 1996;132:640-651.
ABSTRACT  

Keratitis, Ichthyosis, and Deafness (KID) Syndrome: Suggested Changes in Terminology
Myskowski and Nowell
Arch Dermatol 1988;124:22-22.
ABSTRACT  





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