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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease muscular atrophy
Comorbidity C0026848|myopathy
Sentences 13
PubMedID- 22923418 Conclusions: x-linked myopathy with postural muscle atrophy patients consistently showed electrical, functional, and characteristic morphological cardiac abnormalities that translate into reduced exercise capacity.
PubMedID- 21860784 Myositis and myopathy with muscle atrophy are seen in some thymoma mg patients [22].
PubMedID- 20874719 Five other fhl1 mutations were discovered to be causal for x-linked myopathy with postural muscle atrophy (xmpma), clinically characterized by the combined presentation of weakness and atrophy of postural muscles (scapuloperoneal weakness and bent spine) with a pseudoathletic phenotype where alternative muscle groups were hypertrophic [39].
PubMedID- 24391882 It is well known that glucocorticoids at pharmacological levels or in spontaneous cushing’s syndrome cause myopathy, with a combination of muscle atrophy and dysfunction.
PubMedID- 24083177 [315] chronic myopathy can lead to muscle atrophy that regresses only after a matter of weeks or months.
PubMedID- 22053194 Mutations in the fhl1 gene are causative for several types of hereditary myopathies including x-linked myopathy with postural muscle atrophy (xmpma).
PubMedID- 21897683 Probably due to severe muscle wasting, which is not common in patients with cidp, except with concomitant myopathy, the referral diagnosis of spinal muscular atrophy was earlier entertained.
PubMedID- 24125563 Sporadic inclusion body myositis (sibm) is a slowly progressive, red-rimmed vacuolar myopathy leading to muscular atrophy and progressive weakness; it predominantly affects males older than fifty years, and is resistant to immunotherapy.
PubMedID- 22172421 Important new characterizations include 4 distinct human myopathies: reducing body myopathy, x-linked myopathy with postural muscle atrophy, emery-dreifuss muscular dystrophy, and scapuloperoneal myopathy.
PubMedID- 25740800 Critical illness myopathy (cim) is associated with severe muscle atrophy and fatigue in affected patients.
PubMedID- 21932316 Fhl1 mutations cause emery-dreifuss muscular dystrophy (omim 310300), x-linked myopathy with postural muscle atrophy (xmpma, omim 300696), scapuloperoneal myopathy (omim 300695), or reducing body myopathy (omim 300717, 300718).
PubMedID- 24079533 Malnutrition, muscular atrophy, steroid-induced myopathy, pulmonary hyperinflation and reduced blood flow to the respiratory muscles are contributing factors to respiratory muscle weakness in copd patients [29-31].
PubMedID- 24015050 This type of muscular sarcoidosis seems to be chronic myopathy with muscle wasting.

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