Literature DB >> 32147743

Ichthyosis: A Road Model for Skin Research.

Anders Vahlquist1, Hans Törmä.   

Abstract

The understanding of monogenetic disorders of cornification, including the group of diseases called ichthyoses, has expanded greatly in recent years. Studies of the aetiology of more than 50 types of ichthyosis have almost invariably uncovered errors in the biosynthesis of epidermal lipids or structural proteins essential for normal skin barrier function. The barrier abnormality per se may elicit epidermal inflammation, hyperproliferation and hyperkeratosis, potentially contributing to the patient's skin symptoms. Despite this and other new knowledge about pathomechanisms, treatment of ichthyosis often remains unsatisfactory. This review highlights a series of approaches used to elucidate the pathobiology and clinical consequences of different types of ichthyosis, and related diseases with the ultimate goal of finding new and better treatments.

Entities:  

Keywords:  ARCI; ceramides; congenital; epidermolytic; human epidermis; keratinocytes; keratins; therapy; skin pH

Mesh:

Year:  2020        PMID: 32147743      PMCID: PMC9128938          DOI: 10.2340/00015555-3433

Source DB:  PubMed          Journal:  Acta Derm Venereol        ISSN: 0001-5555            Impact factor:   3.875


  100 in total

1.  Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome.

Authors:  N A Schlipf; A Vahlquist; N Teigen; M Virtanen; A Dragomir; S Fismen; M Barenboim; T Manke; B Rösler; A Zimmer; J Fischer
Journal:  Br J Dermatol       Date:  2015-11-19       Impact factor: 9.302

Review 2.  Corneocyte lipid envelope (CLE), the key structure for skin barrier function and ichthyosis pathogenesis.

Authors:  Masashi Akiyama
Journal:  J Dermatol Sci       Date:  2017-06-08       Impact factor: 4.563

3.  Membrane structural abnormalities in the stratum corneum of the autosomal recessive ichthyoses.

Authors:  R Ghadially; M L Williams; S Y Hou; P M Elias
Journal:  J Invest Dermatol       Date:  1992-12       Impact factor: 8.551

4.  Retinoid concentrations in skin, serum and adipose tissue of patients treated with etretinate.

Authors:  O Rollman; A Vahlquist
Journal:  Br J Dermatol       Date:  1983-10       Impact factor: 9.302

5.  Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.

Authors:  Maritta Hellström Pigg; Anette Bygum; Agneta Gånemo; Marie Virtanen; Flemming Brandrup; Andreas D Zimmer; Alrun Hotz; Anders Vahlquist; Judith Fischer
Journal:  Acta Derm Venereol       Date:  2016-11-02       Impact factor: 4.437

6.  Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.

Authors:  J Dahlqvist; J Klar; I Hausser; I Anton-Lamprecht; M Hellström Pigg; T Gedde-Dahl; A Gånemo; A Vahlquist; N Dahl
Journal:  J Med Genet       Date:  2007-06-08       Impact factor: 6.318

7.  The pH gradient over the stratum corneum differs in X-linked recessive and autosomal dominant ichthyosis: a clue to the molecular origin of the "acid skin mantle"?

Authors:  H Ohman; A Vahlquist
Journal:  J Invest Dermatol       Date:  1998-10       Impact factor: 8.551

8.  Clinical, light and electron microscopic features of recessive ichthyosis congenita type III.

Authors:  K M Niemi; L Kanerva; C F Wahlgren; J Ignatius
Journal:  Arch Dermatol Res       Date:  1992       Impact factor: 3.017

9.  Darier's disease and vitamin A. Concentrations of retinoids in serum and epidermis of untreated patients.

Authors:  A Vahlquist; J B Lee; G Michaëlsson
Journal:  Arch Dermatol       Date:  1982-06

10.  Filaggrin loss-of-function mutations are associated with early-onset eczema, eczema severity and transepidermal water loss at 3 months of age.

Authors:  C Flohr; K England; S Radulovic; W H I McLean; L E Campbel; J Barker; M Perkin; G Lack
Journal:  Br J Dermatol       Date:  2010-12       Impact factor: 9.302

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  4 in total

1.  Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian Patients.

Authors:  Tiziana Fioretti; Luigi Auricchio; Angelo Piccirillo; Giuseppina Vitiello; Adelaide Ambrosio; Fabio Cattaneo; Rosario Ammendola; Gabriella Esposito
Journal:  Diagnostics (Basel)       Date:  2020-11-24

Review 2.  Mammalian Epidermis: A Compendium of Lipid Functionality.

Authors:  Matteo Vietri Rudan; Fiona M Watt
Journal:  Front Physiol       Date:  2022-01-12       Impact factor: 4.566

3.  Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation.

Authors:  Mariem Ennouri; Andreas D Zimmer; Emna Bahloul; Rim Chaabouni; Slaheddine Marrakchi; Hamida Turki; Faiza Fakhfakh; Noura Bougacha-Elleuch; Judith Fischer
Journal:  BMC Med Genomics       Date:  2022-01-05       Impact factor: 3.063

4.  Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis.

Authors:  Gregorio Serra; Luigi Memo; Paola Cavicchioli; Mario Cutrone; Mario Giuffrè; Maria Laura La Torre; Ingrid Anne Mandy Schierz; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2022-08-13       Impact factor: 3.288

  4 in total

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