Ontology highlight
ABSTRACT:
SUBMITTER: Mateus T
PROVIDER: S-EPMC8038712 | biostudies-literature | 2021 Apr
REPOSITORIES: biostudies-literature
Mateus Tiago T Almeida Idália I Costa Adriana A Viegas Diana D Magalhães Sandra S Martins Filipa F Herdeiro Maria Teresa MT da Cruz E Silva Odete A B OAB Fraga Carla C Alves Ivânia I Nunes Alexandra A Rebelo Sandra S
International journal of environmental research and public health 20210406 7
Myotonic dystrophy type 1 (DM1) is a hereditary disease characterized by progressive distal muscle weakness and myotonia. Patients with DM1 have abnormal lipid metabolism and a high propensity to develop a metabolic syndrome in comparison to the general population. It follows that metabolome evaluation in these patients is crucial and may contribute to a better characterization and discrimination between DM1 disease phenotypes and severities. Several experimental approaches are possible to carry ...[more]