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Aktuelle Dermatologie 2016; 42(08/09): 332-335
DOI: 10.1055/s-0042-108020
Eine Klinik im Blickpunkt
© Georg Thieme Verlag KG Stuttgart · New York

Keratitis-ichthyosis-deafness (KID)-Syndrom – Fallbericht einer seltenen hereditären Ichthyoseform

Keratitis-ichthyosis-deafness (KID) Syndrome – Case Report of a Rare Hereditary Type of Ichthyosis
S. Dengler
1   Klinik für Dermatologie und Allergologie, Klinikum Dortmund gGmbH
,
V. Oji
2   Klinik für Hautkrankheiten – Allgemeine Dermatologie und Venerologie, Universitätsklinikum Münster, Münster
,
A. Lücke
3   Pathologisches Institut, Klinikum Dortmund gGmbH
,
V. Schindler
4   Hautarztpraxis Dr. med. Volkhard Schindler, Arnsberg
,
D. Nashan
1   Klinik für Dermatologie und Allergologie, Klinikum Dortmund gGmbH
,
H. F. Ständer
1   Klinik für Dermatologie und Allergologie, Klinikum Dortmund gGmbH
5   Dermatologie Bad Bentheim, Praxis für Dermatologie, Bad Bentheim
› Author Affiliations
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Publication History

Publication Date:
18 August 2016 (online)

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Zusammenfassung

Wir berichten über einen 56-jährigen Vater und seinen 18-jährigen Sohn, die beide seit Geburt an der seltenen, autosomal-dominanten Ichthyoseform des Keratitis-Ichthyosis-Taubheit-Syndroms (engl. Keratitis-ichthyosis-deafness (KID) (Syn.: Ichthyosis hystrix Typ Rheydt) leiden. Das Syndrom und die Notwendigkeit intensivierter topischer Behandlungsmaßnahmen, wie auch die dermatochirurgischen Therapieerfolge, werden im Kontext der aktuellen Literatur diskutiert.

Abstract

We report on a 56-year-old father and his 18-year-old son, who both suffer from the rare autosomal dominant type of ichthyosis called keratitis-ichthyosis-deafness (KID) syndrome. The syndrome, the necessity of intensive topical treatment and the successful dermatochirurgical treatment will be discussed in context to the current literature.

 

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