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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease myopathy
Comorbidity C0026848|myopathies
Sentences 11
PubMedID- 22754704 Clinical evidence is lacking in surveillance techniques and protocols tailored to specific neuromuscular diseases, particularly with congenital myopathies, due to the sparse data for the natural disease progression [6].
PubMedID- 23642286 Introduction: idiopathic myopathies are a group of acquired muscular diseases considered as autoimmune disorders.
PubMedID- 23394784 The congenital myopathies are a group of inherited neuromuscular disorders mainly defined on the basis of characteristic histopathological features.
PubMedID- 23273262 Congenital myopathies, a heterogeneous group of muscle disorders defined by distinctive morphologic abnormalities in skeletal muscle fibers, are often caused by structural defects in sarcomeric or cytoskeletal proteins [11].
PubMedID- 24860823 Inflammatory myopathies are another class of chronic muscle diseases.
PubMedID- 21365201 Opinion statement: the inflammatory myopathies, a group of chronic myopathic conditions, are potentially treatable, so proper diagnosis and early initiation of therapy are necessary.
PubMedID- 22577940 The inflammatory myopathies are a group of acquired skeletal muscle diseases that include polymyositis (pm), dermatomyositis (dm), inclusion body myositis, and overlap and cancer-associated myositis.
PubMedID- 23568993 Idiopathic inflammatory myopathies are a group of acquired skeletal muscle diseases that include polymyositis, dermatomyositis, and inclusion body myositis.
PubMedID- 24594700 Idiopathic inflammatory myopathies are a group of acquired muscular disorders including polymyositis (pm), dermatomyositis (dm), immune-mediated necrotizing myopathies (imnm), and sporadic inclusion body myositis (sibm).
PubMedID- 20422195 Dysferlinopathies, which are genetically characterised by mutations in the dysferlin gene lead to lgmd 2b, distal miyoshi myopathies and a form of distal anterior compartment myopathy [42, 43].
PubMedID- 22752422 Congenital myopathies describe a group of inherited muscle disorders with neonatal or infantile onset typically associated with muscle weakness, respiratory involvement and delayed motor milestones.

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