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Congenital and Childhood Myotonic Dystrophy type 1 - the impact on central nervous system, visual and motor function
Background and aims: Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder, caused by an expanded CTG repeat on chromosome 19. The disorder can present both in children and adults. The overall ...
Orofacial dysfunctions in children and adolescents with myotonic dystrophy type 1 - evaluation and intervention
Myotonic dystrophy type 1 (DM1) is a slowly progressive neuromuscular disease. The overall aim of this thesis was primarily to describe the characteristics, prevalence, and development of orofacial functions in a group of ...