For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of
morbidity and mortality. The management of cardiac disease in NMDs is made challenging …

Pediatric neuromuscular diseases encompass all disorders with onset in childhood and
where the primary area of pathology is in the peripheral nervous system. These conditions …

Background: Cardiac troponins are often elevated in patients with skeletal muscle disease
who have no evidence of cardiac disease. Objectives: The goal of this study was to …

Myotonic dystrophy type 1 (DM1) is a multisystem disorder that affects skeletal and smooth
muscle as well as the eye, heart, endocrine system, and central nervous system. The clinical …

Myotonic dystrophy type 1 (DM1) is a multisystemic disorder of genetic origin. Progressive
muscular weakness, atrophy and myotonia are its most prominent neuromuscular features …

Myotonic dystrophy is an autosomal dominant muscular dystrophy not only associated with
muscle weakness, atrophy, and myotonia but also prominent multisystem involvement …

Opinion statement Myotonic dystrophy (DM1) is the most common form of adult muscular
dystrophy. It is a multisystem disorder with a complex pathophysiology. Although inheritance …

Background and objectives Steinert's disease or myotonic dystrophy type 1 (MD1),(OMIM
160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with …

Antecedentes y objetivos La enfermedad de Steinert o distrofia miotónica tipo 1
(DM1),(OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad …

Myotonic dystrophy (DM) is the most common autosomal dominant muscular dystrophy and
encompasses both skeletal muscle and cardiac complications. DM is nucleotide repeat …