Literature DB >> 21191406

Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.

Shirli Israeli, Hadas Zamir, Ofer Sarig, Reuven Bergman, Eli Sprecher.   

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Year:  2010        PMID： 21191406     DOI： 10.1038/jid.2010.363

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  10 in total

1.  Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome.

Authors:  Rita M Cabral; Mazen Kurban; Muhammad Wajid; Yutaka Shimomura; Lynn Petukhova; Angela M Christiano
Journal:  Genomics       Date:  2012-01-25       Impact factor: 5.736

Review 2.  The atopic march: current insights into skin barrier dysfunction and epithelial cell-derived cytokines.

Authors:  Hongwei Han; Florence Roan; Steven F Ziegler
Journal:  Immunol Rev       Date:  2017-07       Impact factor: 12.988

3.  Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A.

Authors:  Janan Mohamad; Ofer Sarig; Lisa M Godsel; Alon Peled; Natalia Malchin; Ron Bochner; Dan Vodo; Tom Rabinowitz; Mor Pavlovsky; Shahar Taiber; Maya Fried; Marina Eskin-Schwartz; Siwar Assi; Noam Shomron; Jouni Uitto; Jennifer L Koetsier; Reuven Bergman; Kathleen J Green; Eli Sprecher
Journal:  J Invest Dermatol       Date:  2018-06-27       Impact factor: 8.551

Review 4.  Inborn errors of immunity with atopic phenotypes: A practical guide for allergists.

Authors:  Riccardo Castagnoli; Vassilios Lougaris; Giuliana Giardino; Stefano Volpi; Lucia Leonardi; Francesco La Torre; Silvia Federici; Stefania Corrente; Bianca Laura Cinicola; Annarosa Soresina; Caterina Cancrini; Gian Luigi Marseglia; Fabio Cardinale
Journal:  World Allergy Organ J       Date:  2021-02-22       Impact factor: 4.084

Review 5.  Skin barrier disruption: a requirement for allergen sensitization?

Authors:  Anna De Benedetto; Akiharu Kubo; Lisa A Beck
Journal:  J Invest Dermatol       Date:  2012-01-05       Impact factor: 8.551

Review 6.  Epidermal barrier disorders and corneodesmosome defects.

Authors:  Marek Haftek
Journal:  Cell Tissue Res       Date:  2014-11-07       Impact factor: 5.249

7.  Adult-onset acral peeling skin syndrome in a non-identical twin: a case report in South Africa.

Authors:  Reshmi Mathew; Olufemi B Omole; Jonathan Rigby; Wayne Grayson
Journal:  Am J Case Rep       Date:  2014-12-31

8.  A Case of Inflammatory Generalized Type of Peeling Skin Syndrome Possibly Caused by a Homozygous Missense Mutation of CDSN.

Authors:  Hiroshi Kawakami; Masaki Uchiyama; Tatsuo Maeda; Takahiko Tsunoda; Yoshihiko Mitsuhashi; Ryoji Tsuboi
Journal:  Case Rep Dermatol       Date:  2014-10-11

9.  Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin.

Authors:  Maeve A McAleer; Elizabeth Pohler; Frances J D Smith; Neil J Wilson; Christian Cole; Stuart MacGowan; Jennifer L Koetsier; Lisa M Godsel; Robert M Harmon; Robert Gruber; Debra Crumrine; Peter M Elias; Michael McDermott; Karina Butler; Annemarie Broderick; Ofer Sarig; Eli Sprecher; Kathleen J Green; W H Irwin McLean; Alan D Irvine
Journal:  J Allergy Clin Immunol       Date:  2015-06-12       Impact factor: 10.793

10.  A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.

Authors:  Helen Gordon; Patrick Yap; Kuang-Chih Hsiao; Michael Watson; Diana Purvis
Journal:  Pediatr Dermatol       Date:  2022-02-17       Impact factor: 1.997
  10 in total

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