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Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients.
dc.rights.license | open | en_US |
dc.contributor.author | BESSIS, Didier | |
dc.contributor.author | BURSZTEJN, Anne-Claire | |
hal.structure.identifier | Service de dermatologie [Bordeaux] | |
hal.structure.identifier | Hôpital Pellegrin | |
hal.structure.identifier | Service de génétique médicale | |
hal.structure.identifier | Service de dermatologie Hôpital Saint-André Bordeaux | |
hal.structure.identifier | Centre Hospitalier Universitaire de Bordeaux [CHU Bordeaux] | |
hal.structure.identifier | CHU de Bordeaux Pellegrin [Bordeaux] | |
hal.structure.identifier | Thérapie génique, Génomique et Epigénomique [U 1169] | |
hal.structure.identifier | Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM] | |
dc.contributor.author | MORICE-PICARD, Fanny | |
dc.contributor.author | CAPRI, Yline | |
dc.contributor.author | BARBAROT, Sébastien | |
dc.contributor.author | AUBERT, Hélène | |
dc.contributor.author | BODET, Damien | |
dc.contributor.author | BOURRAT, Emmanuelle | |
dc.contributor.author | CHIAVERINI, Christine | |
dc.contributor.author | POUJADE, Laura | |
dc.contributor.author | WILLEMS, Marjolaine | |
dc.contributor.author | ROUANET, Jacques | |
dc.contributor.author | DOMPMARTIN-BLANCHÈRE, Anne | |
dc.contributor.author | GENEVIÈVE, David | |
dc.contributor.author | GERARD, Marion | |
dc.contributor.author | GINGLINGER, Emmanuelle | |
dc.contributor.author | HADJ-RABIA, Smaïl | |
dc.contributor.author | MARTIN, Ludovic | |
dc.contributor.author | MAZEREEUW-HAUTIER, Juliette | |
dc.contributor.author | BIBAS, Nathalie | |
dc.contributor.author | MOLINARI, Nicolas | |
dc.contributor.author | HERMAN, Fanchon | |
dc.contributor.author | PHAN, Alice | |
dc.contributor.author | ROD, Julien | |
dc.contributor.author | ROGER, Hugues | |
dc.contributor.author | SIGAUDY, Sabine | |
dc.contributor.author | ZIEGLER, Alban | |
dc.contributor.author | VIAL, Yoann | |
dc.contributor.author | VERLOES, Alain | |
dc.contributor.author | CAVÉ, Hélène | |
hal.structure.identifier | Hôpital Pellegrin | |
hal.structure.identifier | Service de génétique médicale | |
hal.structure.identifier | Centre Hospitalier Universitaire de Bordeaux [CHU Bordeaux] | |
hal.structure.identifier | Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM] | |
dc.contributor.author | LACOMBE, Didier | |
dc.date.accessioned | 2024-07-18T07:55:28Z | |
dc.date.available | 2024-07-18T07:55:28Z | |
dc.date.issued | 2024-04-10 | |
dc.identifier.issn | 1468-3083 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/201019 | |
dc.description.abstractEn | Data on dermatological manifestations of Costello syndrome (CS) remain heterogeneous and lack in validated description. To describe the dermatological manifestations of CS; compare them with the literature findings; assess those discriminating CS from other RASopathies, including cardiofaciocutaneous syndrome (CFCS) and the main types of Noonan syndrome (NS); and test for dermatological phenotype-genotype correlations. We performed a 10-year, large, prospective, multicentric, collaborative dermatological and genetic study. Thirty-one patients were enrolled. Hair abnormalities were ubiquitous, including wavy or curly hair and excessive eyebrows, respectively in 68% and 56%. Acral excessive skin (AES), papillomas and keratotic papules (PKP), acanthosis nigricans (AN), palmoplantar hyperkeratosis (PPHK) and 'cobblestone' papillomatous papules of the upper lip (CPPUL), were noted respectively in 84%, 61%, 65%, 55% and 32%. Excessive eyebrows, PKP, AN, CCPUL and AES best differentiated CS from CFCS and NS. Multiple melanocytic naevi (>50) may constitute a new marker of attenuated CS associated with intragenic duplication in HRAS. Oral acitretin may be highly beneficial for therapeutic management of PPHK. No significant dermatological phenotype-genotype correlation was determined between patients with and without HRAS c.34G>A (p.G12S). This validated phenotypic characterization of a large number of patients with CS will allow future researchers to make a positive diagnosis, and to differentiate CS from CFCS and NS. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.title.en | Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. | |
dc.title.alternative | J Eur Acad Dermatol Venereol | en_US |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1111/jdv.19996 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Médecine humaine et pathologie/Dermatologie | en_US |
dc.identifier.pubmed | 38595321 | en_US |
bordeaux.journal | Journal of the European Academy of Dermatology and Venereology | en_US |
bordeaux.hal.laboratories | Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
bordeaux.import.source | pubmed | |
hal.popular | non | en_US |
hal.audience | Internationale | en_US |
hal.export | false | |
workflow.import.source | pubmed | |
dc.rights.cc | CC BY-NC-ND | en_US |
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