TY - JOUR
T1 - Revised nomenclature and classification of inherited ichthyoses
T2 - Results of the First Ichthyosis Consensus Conference in Sorèze 2009
AU - Oji, Vinzenz
AU - Tadini, Gianluca
AU - Akiyama, Masashi
AU - Blanchet Bardon, Claudine
AU - Bodemer, Christine
AU - Bourrat, Emmanuelle
AU - Coudiere, Philippe
AU - DiGiovanna, John J
AU - Elias, Peter
AU - Fischer, Judith
AU - Fleckman, Philip
AU - Gina, Michal
AU - Harper, John
AU - Hashimoto, Takashi
AU - Hausser, Ingrid
AU - Hennies, Hans Christian
AU - Hohl, Daniel
AU - Hovnanian, Alain
AU - Ishida-Yamamoto, Akemi
AU - Jacyk, Witold K
AU - Leachman, Sancy
AU - Leigh, Irene
AU - Mazereeuw-Hautier, Juliette
AU - Milstone, Leonard
AU - Morice-Picard, Fanny
AU - Paller, Amy S
AU - Richard, Gabriele
AU - Schmuth, Matthias
AU - Shimizu, Hiroshi
AU - Sprecher, Eli
AU - van Steensel, Maurice
AU - Taïeb, Alain
AU - Toro, Jorge R
AU - Vabres, Pierre
AU - Vahlquist, Anders
AU - Williams, Mary
AU - Traupe, Heiko
N1 - Copyright © 2010 American Academy of Dermatology, Inc. All rights reserved.
PY - 2010/10
Y1 - 2010/10
N2 - 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 Sorèze, 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.
AB - 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 Sorèze, 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.
KW - Adolescent
KW - Adult
KW - Child
KW - Congresses as Topic
KW - Dermatologic Agents
KW - Female
KW - France
KW - Gene Expression Regulation
KW - Genetic Predisposition to Disease
KW - Humans
KW - Ichthyosiform Erythroderma, Congenital
KW - Ichthyosis
KW - Infant
KW - Infant, Newborn
KW - Male
KW - Practice Guidelines as Topic
KW - Prognosis
KW - Severity of Illness Index
KW - Terminology as Topic
KW - Young Adult
KW - Journal Article
KW - Research Support, Non-U.S. Gov't
KW - Review
U2 - 10.1016/j.jaad.2009.11.020
DO - 10.1016/j.jaad.2009.11.020
M3 - Review article
C2 - 20643494
VL - 63
SP - 607
EP - 641
JO - Journal of the American Academy of Dermatology
JF - Journal of the American Academy of Dermatology
SN - 0190-9622
IS - 4
ER -