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dc.contributor.authorMcCarthy, RL
dc.contributor.authorde Brito, M
dc.contributor.authorO'Toole, EA
dc.date.accessioned2024-05-31T12:17:44Z
dc.date.available2024-05-27
dc.date.available2024-05-31T12:17:44Z
dc.date.issued2024-05-28
dc.identifier.citationRebecca L McCarthy, Marianne de Brito, Edel A O’Toole, Pachyonychia congenita – pathogenesis of pain and approaches to treatment, Clinical and Experimental Dermatology, 2024;, llae199, https://doi.org/10.1093/ced/llae199en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/97144
dc.description.abstractPachyonychia congenita is an autosomal dominant genodermatosis characterized by a triad of chronic severe plantar pain, focal palmoplantar keratoderma, and hypertrophic nail dystrophy. Plantar pain can be debilitating and have a profound impact on quality of life. Current therapeutic options for pain in PC are limited to lifestyle adjustment and mechanical techniques, with a small subgroup of patients benefiting from oral retinoids. This review investigates the pathogenesis of pain in pachyonychia congenita and provides a summary of the current and future therapeutic options.en_US
dc.languageeng
dc.publisherOxford University Pressen_US
dc.relation.ispartofClin Exp Dermatol
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.titlePachyonychia congenita - pathogenesis of pain and approaches to treatment.en_US
dc.typeArticleen_US
dc.rights.holder© The Author(s) 2024. Published by Oxford University Press on behalf of British Association of Dermatologists.
dc.identifier.doi10.1093/ced/llae199
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38805703en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
dcterms.dateAccepted2024-05-27
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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