作者: T. Barba , J.-C. Boileau , F. Pasquet , A. Hot , M. Pavic
DOI: 10.1016/J.REVMED.2015.12.022
关键词:
摘要: Myeloproliferative disorders and secondary polycythemia cover most of the cases encountered in daily practice. Inherited polycythemias are rare entities that have to be suspected when classical causes acquired been ruled out. Recent advances were made understanding these pathologies, which still little known physicians. This review reports state knowledge proposes an algorithm follow confronted a possible case inherited polycythemia.