Literature DB >> 31642606

Spectrum of ichthyoses in an Austrian ichthyosis cohort from 2004 to 2017.

Magdalena Seidl-Philipp1, Ulrich A Schatz2, Irina Gasslitter3, Verena Moosbrugger-Martinz1, Stefan Blunder1, Anna S Schossig2, Johannes Zschocke2, Matthias Schmuth1, Robert Gruber1.   

Abstract

BACKGROUND: Ichthyoses are a heterogeneous disease group, which makes clinical classification challenging. An ichthyosis cohort at a center for genodermatoses is presented in detail. PATIENTS AND METHODS: Patients with clinically and/or genetically confirmed ichthyosis seen from 2004 to 2017 and listed in a database were included. Disease onset, phenotype, histology, comorbidities and family history were described in detail. In genetically tested patients, the prevalence of various ARCI genes, ARCI phenotypes and syndromic ichthyoses, as well as genotype-phenotype correlation and year/method of genetic testing was assessed.
RESULTS: Of all 198 patients who were included in the cohort, 151 were genetically tested. 81 had ichthyosis vulgaris, 43 X-linked ichthyosis, 38 autosomal recessive congenital ichthyosis (ARCI), 9 keratinopathic ichthyosis (KPI) and one exfoliative ichthyosis. 26 individuals suffered from syndromic ichthyoses. A good genotype-phenotype correlation was observed for common ichthyoses and KPI; the correlation was less good in syndromic ichthyoses. In 91 % of ARCI patients an accurate diagnosis was obtained by genetic testing. In only 33 % of syndromic ichthyoses was the definitive diagnosis suspected before genetic testing, which revealed a causative mutation in 86 % of cases.
CONCLUSION: This study describes the spectrum of ichthyoses in a center of expertise and shows that genetic testing should become a diagnostic standard for this disease group.
© 2019 The Authors. Journal der Deutschen Dermatologischen Gesellschaft published by John Wiley & Sons Ltd on behalf of Deutsche Dermatologische Gesellschaft.

Entities:  

Year:  2019        PMID: 31642606     DOI: 10.1111/ddg.13968

Source DB:  PubMed          Journal:  J Dtsch Dermatol Ges        ISSN: 1610-0379            Impact factor:   5.584


  3 in total

1.  Mild Phenotype of Arthrogryposis, Renal Dysfunction, and Cholestasis Syndrome 1 Caused by a Novel VPS33B Variant.

Authors:  Natália Duarte Linhares; Eleonora Druve Tavares Fagundes; Alexandre Rodrigues Ferreira; Thaís Costa Nascentes Queiroz; Luiz Roberto da Silva; Sergio D J Pena
Journal:  Front Genet       Date:  2022-02-25       Impact factor: 4.599

2.  Developmental cell programs are co-opted in inflammatory skin disease.

Authors:  Gary Reynolds; Peter Vegh; James Fletcher; Elizabeth F M Poyner; Emily Stephenson; Issac Goh; Rachel A Botting; Ni Huang; Bayanne Olabi; Anna Dubois; David Dixon; Kile Green; Daniel Maunder; Justin Engelbert; Mirjana Efremova; Krzysztof Polański; Laura Jardine; Claire Jones; Thomas Ness; Dave Horsfall; Jim McGrath; Christopher Carey; Dorin-Mirel Popescu; Simone Webb; Xiao-Nong Wang; Ben Sayer; Jong-Eun Park; Victor A Negri; Daria Belokhvostova; Magnus D Lynch; David McDonald; Andrew Filby; Tzachi Hagai; Kerstin B Meyer; Akhtar Husain; Jonathan Coxhead; Roser Vento-Tormo; Sam Behjati; Steven Lisgo; Alexandra-Chloé Villani; Jaume Bacardit; Philip H Jones; Edel A O'Toole; Graham S Ogg; Neil Rajan; Nick J Reynolds; Sarah A Teichmann; Fiona M Watt; Muzlifah Haniffa
Journal:  Science       Date:  2021-01-22       Impact factor: 47.728

3.  Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis.

Authors:  Fozia Fozia; Rubina Nazli; Sher Alam Khan; Ahmed Bari; Abdul Nasir; Riaz Ullah; Hafiz Majid Mahmood; Muhammad Sohaib; Abdulrahman Alobaid; Siddique A Ansari; Sulman Basit; Saadullah Khan
Journal:  Genes (Basel)       Date:  2021-03-05       Impact factor: 4.096

  3 in total

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