PT - JOURNAL ARTICLE AU - Rodríguez-López, Claudia AU - García-Cárdaba, Luis M. AU - Blázquez, Alberto AU - Serrano-Lorenzo, Pablo AU - Gutiérrez-Gutiérrez, Gerardo AU - San Millán-Tejado, Beatriz AU - Muelas, Nuria AU - Hernández-Laín, Aurelio AU - Vílchez, Juan J. AU - Gutiérrez-Rivas, Eduardo AU - Arenas, Joaquín AU - Martín, Miguel A. AU - Domínguez-González, Cristina TI - Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia AID - 10.1136/jmedgenet-2019-106649 DP - 2020 Sep 01 TA - Journal of Medical Genetics PG - 643--646 VI - 57 IP - 9 4099 - http://jmg.bmj.com/content/57/9/643.short 4100 - http://jmg.bmj.com/content/57/9/643.full SO - J Med Genet2020 Sep 01; 57 AB - Background Mitochondrial progressive external ophthalmoplegia (PEO) encompasses a broad spectrum of clinical and genetic disorders. We describe the phenotypic subtypes of PEO and its correlation with molecular defects and propose a diagnostic algorithm.Methods Retrospective analysis of the clinical, pathological and genetic features of 89 cases.Results Three main phenotypes were found: ‘pure PEO’ (42%), consisting of isolated palpebral ptosis with ophthalmoparesis; Kearns-Sayre syndrome (10%); and ‘PEO plus’, which associates extraocular symptoms, distinguishing the following subtypes: : myopathic (33%), bulbar (12%) and others (3%). Muscle biopsy was the most accurate test, showing mitochondrial changes in 95%. Genetic diagnosis was achieved in 96% of the patients. Single large-scale mitochondrial DNA (mtDNA) deletion was the most frequent finding (63%), followed by multiple mtDNA deletions (26%) due to mutations in TWNK (n=8), POLG (n=7), TK2 (n=6) or RRM2B (n=2) genes, and point mtDNA mutations (7%). Three new likely pathogenic mutations were identified in the TWNK and MT-TN genes.Conclusions Phenotype–genotype correlations cannot be brought in mitochondrial PEO. Muscle biopsy should be the first step in the diagnostic flow of PEO when mitochondrial aetiology is suspected since it also enables the study of mtDNA rearrangements. If no mtDNA deletions are identified, whole mtDNA sequencing should be performed.