| Literature DB >> 33491095 |
Sabine Jägle1, Hazem A Juratli, Geoffroy Hickman, Kira Süssmuth, Maria C Boente, Julia Kopp, Peter Kirchmeier, Andreas Zimmer, Rudolf Happle, Emmanuelle Bourrat, Henning Hamm, Judith Fischer.
Abstract
Porokeratoses are a heterogeneous group of keratinization disorders. For linear porokeratosis and disseminated superficial actinic porokeratosis, a heterozygous pathogenic germline variant in a mevalonate pathway gene and a postzygotic second hit mutation present in affected skin have been shown to be the patho-genetic mechanism for the development of the lesions. However, the molecular mechanism leading to development of porokeratosis plantaris, palmaris et disseminata is not known. This study analysed a cohort of 4 patients with linear porokeratosis and 3 patients with porokeratosis plantaris, palmaris et disseminata, and performed mutation analyses of DNA extracted from blood samples and skin biopsies. All of the study patients carried the heterozygous germline variant c.70+5G>A in the MVD gene. Loss of heterozygosity due to a second hit mutation was found in affected skin of 3 patients with linear porokeratosis and 2 patients with porokeratosis plantaris, palmaris et disseminata. These results suggest that porokeratosis plantaris, palmaris et disseminata shares the same pathogenetic mechanism as other porokeratosis subtypes and belongs to the phenotypic spectrum of MVD-associated porokeratosis.Entities:
Keywords: linear porokeratosis; loss of heterozygosity; mosaicism; palmaris et disseminata; porokeratosis plantaris; second hit; mevalonate diphosphate decarboxylase gene
Mesh:
Year: 2021 PMID: 33491095 PMCID: PMC9366687 DOI: 10.2340/00015555-3753
Source DB: PubMed Journal: Acta Derm Venereol ISSN: 0001-5555 Impact factor: 3.875