| Literature DB >> 32147747 |
Judith Fischer1, Emmanuelle Bourrat.
Abstract
Inherited ichthyoses are classified as Mendelian disorders of cornification (MEDOC), which are defined on the basis of clinical and genetic features and are mainly divided into non-syndromic and syndromic ichthyoses. Numerous genes, which encode for corresponding proteins, are involved in the normal differentiation of keratinocytes (cornification) and participate in the formation of a functional epidermal barrier. To date, mutations in more than 50 genes are known to result in various types of ichthyoses. Thanks to modern genetic diagnostic methods based on targeted next generation sequencing (NGS), approximately 80-90% of cases can be resolved at present. Further sequencing methods covering the whole exome (WES) or whole genome (WGS) will obviously elucidate another portion of the remaining unknown ichthyoses in the future.Entities:
Keywords: ARCI; genes; ichthyoses; molecular genetic diagnostics; mutations; Mendelian disorders of cornification
Mesh:
Year: 2020 PMID: 32147747 PMCID: PMC9128940 DOI: 10.2340/00015555-3432
Source DB: PubMed Journal: Acta Derm Venereol ISSN: 0001-5555 Impact factor: 3.875