Torres, VivianaPainous Martí, CèliaSantacruz, PilarSánchez, AuroraSanz, CristinaGrau Junyent, Josep M. (Josep Maria)Muñoz, Esteban2022-11-212022-11-212022-07-032330-1619https://hdl.handle.net/2445/191063McLeod syndrome (MLS) is a very rare genetic X-linked condition due to XK gene mutations and characterized by the development of chorea, psychiatric and cognitive impairment, seizures, cardiomyopathy, muscular involvement and the presence of acanthocytes. We present the case of a patient with very long lasting mild myalgia and elevated creatine kinase (CK) who developed lateonset chorea and was finally diagnosed with MLS.4 p.application/pdfengcc by-nc-nd (c) Torres, Viviana et al., 2022http://creativecommons.org/licenses/by-nc-nd/3.0/es/Genètica humanaAnomalies cromosòmiquesCorea de SydenhamCreatina quinasaHematiesHuman geneticsChromosome abnormalitiesChoreaCreatine kinaseErythrocytesinfo:eu-repo/semantics/publishedVersion7238822022-11-21info:eu-repo/semantics/openAccess35937484