Ontology highlight
ABSTRACT:
SUBMITTER: Baldanzi S
PROVIDER: S-EPMC5416743 | biostudies-literature | 2016 Dec
REPOSITORIES: biostudies-literature
Baldanzi Sigrid S Ricci Giulia G Simoncini Costanza C Cosci O Di Coscio Mirna M Siciliano Gabriele G
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 20161201 3
Myotonic dystrophy type 1 (DM1), also called Steinert's disease, is a genetic multisystem disorder that has raised, in the last years, high interest because of the high variable clinical spectrum and related disability. Children with myotonic dystrophy are affected by behavioural problems and intellectual disability, finally impacting on their degree of engagement in family, work and social activities. The transition phase, representing the process of moving from adolescence to adulthood, can be ...[more]