Literature DB >> 20643494

Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.

Vinzenz Oji1, Gianluca Tadini, Masashi Akiyama, Claudine Blanchet Bardon, Christine Bodemer, Emmanuelle Bourrat, Philippe Coudiere, John J DiGiovanna, Peter Elias, Judith Fischer, Philip Fleckman, Michal Gina, John Harper, Takashi Hashimoto, Ingrid Hausser, Hans Christian Hennies, Daniel Hohl, Alain Hovnanian, Akemi Ishida-Yamamoto, Witold K Jacyk, Sancy Leachman, Irene Leigh, Juliette Mazereeuw-Hautier, Leonard Milstone, Fanny Morice-Picard, Amy S Paller, Gabriele Richard, Matthias Schmuth, Hiroshi Shimizu, Eli Sprecher, Maurice Van Steensel, Alain Taïeb, Jorge R Toro, Pierre Vabres, Anders Vahlquist, Mary Williams, Heiko Traupe.   

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 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.
Copyright © 2010 American Academy of Dermatology, Inc. All rights reserved.

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Year:  2010        PMID: 20643494     DOI: 10.1016/j.jaad.2009.11.020

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  158 in total

Review 1.  Inherited ichthyoses/generalized Mendelian disorders of cornification.

Authors:  Matthias Schmuth; Verena Martinz; Andreas R Janecke; Christine Fauth; Anna Schossig; Johannes Zschocke; Robert Gruber
Journal:  Eur J Hum Genet       Date:  2012-06-27       Impact factor: 4.246

Review 2.  [Practical aspects of molecular diagnostics in genodermatoses].

Authors:  C Has; Y He
Journal:  Hautarzt       Date:  2016-01       Impact factor: 0.751

Review 3.  Fatty acid transporters in skin development, function and disease.

Authors:  Meei-Hua Lin; Denis Khnykin
Journal:  Biochim Biophys Acta       Date:  2013-10-08

Review 4.  [Interdisciplinary care of newborns with epidermolysis bullosa and severe congenital ichthyoses].

Authors:  H Ott; F Guthmann; B Ludwikowski
Journal:  Hautarzt       Date:  2015-04       Impact factor: 0.751

5.  Embryonic AP1 Transcription Factor Deficiency Causes a Collodion Baby-Like Phenotype.

Authors:  Christina A Young; Richard L Eckert; Gautam Adhikary; Debra Crumrine; Peter M Elias; Miroslav Blumenberg; Ellen A Rorke
Journal:  J Invest Dermatol       Date:  2017-05-16       Impact factor: 8.551

6.  Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature.

Authors:  Kunal Malik; Helen He; Thy Nhat Huynh; Gary Tran; Kelly Mueller; Kristina Doytcheva; Yael Renert-Yuval; Tali Czarnowicki; Shai Magidi; Margaret Chou; Yeriel D Estrada; Huei-Chi Wen; Xiangyu Peng; Hui Xu; Xiuzhong Zheng; James G Krueger; Amy S Paller; Emma Guttman-Yassky
Journal:  J Allergy Clin Immunol       Date:  2018-05-24       Impact factor: 10.793

Review 7.  Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Authors:  John Timothy Wright; Mary Fete; Holm Schneider; Madelaine Zinser; Maranke I Koster; Angus J Clarke; Smail Hadj-Rabia; Gianluca Tadini; Nina Pagnan; Atila F Visinoni; Birgitta Bergendal; Becky Abbott; Timothy Fete; Clark Stanford; Clayton Butcher; Rena N D'Souza; Virginia P Sybert; Maria I Morasso
Journal:  Am J Med Genet A       Date:  2019-01-31       Impact factor: 2.802

8.  Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)-Deficient Canines.

Authors:  Elizabeth A Mauldin; Debra Crumrine; Margret L Casal; Sekyoo Jeong; Lukáš Opálka; Katerina Vavrova; Yoshikazu Uchida; Kyungho Park; Brittany Craiglow; Keith A Choate; Kyong-Oh Shin; Yong-Moon Lee; Gary L Grove; Joan S Wakefield; Denis Khnykin; Peter M Elias
Journal:  Am J Pathol       Date:  2018-03-13       Impact factor: 4.307

9.  Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.

Authors:  F J D Smith; I M Kreuser-Genis; C S Jury; N J Wilson; A Terron-Kwiatowski; M Zamiri
Journal:  Clin Exp Dermatol       Date:  2018-10-04       Impact factor: 3.470

10.  Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.

Authors:  Rahim Ullah; Muhammad Ansar; Zaka Ullah Durrani; Kwanghyuk Lee; Regie Lyn P Santos-Cortez; Dost Muhammad; Mahboob Ali; Muhammad Zia; Muhammad Ayub; Suliman Khan; Josh D Smith; Deborah A Nickerson; Jay Shendure; Michael Bamshad; Suzanne M Leal; Wasim Ahmad
Journal:  Int J Dermatol       Date:  2015-11-17       Impact factor: 2.736

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