Lo Riso, LauraVargas-Parra, GardeniaNavarro, GemmaArenillas Rocha, LeonorFernández-Ibarrondo, LierniRobredo, BeatrizBallester, CarmenLópez, BernardoPerez-Montaña, AlbertSampol, AntoniaFlorensa Brichs, LourdesBesses Raebel, CarlesDuran, María AntoniaBellosillo Paricio, Beatriz2023-04-052023-04-052022Lo Riso L, Vargas-Parra G, Navarro G, Arenillas L, Fernández-Ibarrondo L, Robredo B, Ballester C, López B, Perez-Montaña A, Sampol A, Florensa L, Besses C, Duran MA, Bellosillo B. Identification of two novel EPOR gene variants in primary familial polycythemia: Case report and literature review. Genes (Basel). 2022 Sep 20;13(10):1686. DOI: 10.3390/genes131016862073-4425http://hdl.handle.net/10230/56413Primary familial and congenital polycythemia is a rare disease characterized by an increase in red cell mass that may be due to pathogenic variants in the EPO receptor (EPOR) gene. To date, 33 genetic variants have been reported to be associated. We analyzed the presence of EPOR variants in two patients with polycythemia in whom JAK2 pathogenic variants had been previously discarded. Molecular analysis of the EPOR gene was performed by Sanger sequencing of the coding regions and exon/intron boundaries of exon 8. We performed in vitro culture of erythroid progenitor cells. Segregation studies were done whenever possible. The two patients studied showed hypersensitivity to EPO in in vitro cultures. Analysis of the EPOR gene unveiled two novel pathogenic variants. Genetic testing of asymptomatic relatives could guarantee surveillance and proper management.application/pdfeng© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).info:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/genes13101686EPORErythrocytosisPolycythemiaVariantsinfo:eu-repo/semantics/openAccess