Genetics and clinical phenotype of Erdheim–Chester disease: A case report of constrictive pericarditis and a systematic review of the literature

BackgroundErdheim–Chester disease (ECD) is a rare form of histiocytosis. An increasing number of genetic mutations have been associated with this syndrome, confirming its possible neoplastic origin. Recently, a connection between the BRAF mutational status and a specific phenotype was described; how...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Lorenzo Bartoli, Francesco Angeli, Andrea Stefanizzi, Michele Fabrizio, Pasquale Paolisso, Luca Bergamaschi, Alessandro Broccoli, Pier Luigi Zinzani, Nazzareno Galiè, Paola Rucci, Alberto Foà, Carmine Pizzi
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Frontiers Media S.A. 2022-08-01
Sarja:	Frontiers in Cardiovascular Medicine
Aiheet:	Erdheim-Chester disease constrictive pericarditis genotype phenotype precision medicine case-report
Linkit:	https://www.frontiersin.org/articles/10.3389/fcvm.2022.876294/full
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