Oji, Vinzenz ORCID: 0000-0003-1380-4828, Tadini, Gianluca, Akiyama, Masashi, Bardon, Claudine Blanchet, Bodemer, Christine, Bourrat, Emmanuelle, Coudiere, Philippe, DiGiovanna, John J., Elias, Peter, Fischer, Judith ORCID: 0000-0002-8580-8118, Fleckman, Philip, Gina, Michal, Harper, John, Hashimoto, Takashi, Hausser, Ingrid, Hennies, Hans Christian, Hohl, Daniel, Hovnanian, Alain ORCID: 0000-0003-3412-7512, Ishida-Yamamoto, Akemi, Jacyk, Witold K., Leachman, Sancy, Leigh, Irene, Mazereeuw-Hautier, Juliette, Milstone, Leonard, Morice-Picard, Fanny, Paller, Amy S., Richard, Gabriele, Schmuth, Matthias ORCID: 0000-0002-4064-1334, Shimizu, Hiroshi, Sprecher, Eli, Van Steensel, Maurice, Taieb, Alain, Toro, Jorge R., Vabres, Pierre ORCID: 0000-0001-8693-3183, Vahlquist, Anders, Williams, Mary and Traupe, Heiko (2010). Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Soreze 2009. J. Am. Acad. Dermatol., 63 (4). S. 607 - 642. NEW YORK: MOSBY-ELSEVIER. ISSN 0190-9622

Full text not available from this repository.

Abstract

Background: Inherited ichthyoses belong to a large, clinically and etiologically heterogeneous group of mendelian disorders of cornification; typically involving the entire integument. Over the recent years, much progress has been made defining their molecular causes. However, there is no internationally accepted classification and terminology. Objective: We sought to establish a consensus for the nomenclature and classification of inherited ichthyoses. Methods: The classification project started at the First World Conference on Ichthyosis in 2007. A large international network of expert clinicians, skin pathologists, and geneticists entertained an interactive dialogue over 2 years, eventually leading to the First Ichthyosis Consensus Conference held in Soreze, France, on January 23 and 24, 2009, where subcommittees on different issues proposed terminology that was debated until consensus was reached. Results: It was agreed that currently the nosology should remain clinically based. Syndromic versus nonsyndromic forms provide a useful major subdivision. Several clinical terms and controversial disease names have been redefined: eg, the group caused by keratin mutations is referred to by the umbrella term, keratinopathic ichthyosis-under which are included epidermolytic ichthyosis, superficial epidermolytic ichthyosis, and ichthyosis Curth-Macklin. Autosomal recessive congenital ichthyosis is proposed as an umbrella term for the harlequin ichthyosis, lamellar ichthyosis, and the congenital ichthyosiform erythroderma group. Limitations: As more becomes known about these diseases in the future, modifications will be needed. Conclusion: We have achieved an international consensus for the classification of inherited ichthyosis that should be useful for all clinicians and can serve as reference point for future research. (I Am Acad Dermatol 2010;63:607-41.)

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Oji, VinzenzUNSPECIFIEDorcid.org/0000-0003-1380-4828UNSPECIFIED
Tadini, GianlucaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Akiyama, MasashiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bardon, Claudine BlanchetUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bodemer, ChristineUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bourrat, EmmanuelleUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Coudiere, PhilippeUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
DiGiovanna, John J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Elias, PeterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fischer, JudithUNSPECIFIEDorcid.org/0000-0002-8580-8118UNSPECIFIED
Fleckman, PhilipUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gina, MichalUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Harper, JohnUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hashimoto, TakashiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hausser, IngridUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hennies, Hans ChristianUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hohl, DanielUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hovnanian, AlainUNSPECIFIEDorcid.org/0000-0003-3412-7512UNSPECIFIED
Ishida-Yamamoto, AkemiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Jacyk, Witold K.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Leachman, SancyUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Leigh, IreneUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mazereeuw-Hautier, JulietteUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Milstone, LeonardUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Morice-Picard, FannyUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Paller, Amy S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Richard, GabrieleUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schmuth, MatthiasUNSPECIFIEDorcid.org/0000-0002-4064-1334UNSPECIFIED
Shimizu, HiroshiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Sprecher, EliUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Van Steensel, MauriceUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Taieb, AlainUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Toro, Jorge R.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Vabres, PierreUNSPECIFIEDorcid.org/0000-0001-8693-3183UNSPECIFIED
Vahlquist, AndersUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Williams, MaryUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Traupe, HeikoUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-495915
DOI: 10.1016/j.jaad.2009.11.020
Journal or Publication Title: J. Am. Acad. Dermatol.
Volume: 63
Number: 4
Page Range: S. 607 - 642
Date: 2010
Publisher: MOSBY-ELSEVIER
Place of Publication: NEW YORK
ISSN: 0190-9622
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
BATHING-SUIT ICHTHYOSIS; EPIDERMAL PERMEABILITY BARRIER; HEALING COLLODION BABY; LIPID STORAGE DISEASE; OF-FUNCTION MUTATIONS; EPIDERMOLYTIC HYPERKERATOSIS; LAMELLAR ICHTHYOSIS; CONGENITAL ICHTHYOSIS; PRENATAL-DIAGNOSIS; NETHERTON-SYNDROMEMultiple languages
DermatologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/49591

Downloads

Downloads per month over past year

Altmetric

Export

Actions (login required)

View Item View Item