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339 Possible Causes for Myopathy, Unable to Stand

  • Muscular Dystrophy

    The majority of individuals are unable to sit or stand without support, and some affected children may never learn to walk.[] Nemaline myopathy Nemaline myopathy. Clusters of rod bodies. Gomori trichrome. Nemaline myopathy Nemaline myopathy. EM.[] I have never been able to walk or stand.[]

  • Duchenne Muscular Dystrophy

    This can result in trouble standing-up. Most are unable to walk by the age of twelve. Affected muscles may look larger due to increased fat content.[] It is associated with a wide variety of myopathic disorders that affect paraspinal muscles, including inflammatory and inherited myopathies.[] Children with Duchenne may be slower to sit, stand or walk. Most are unable to run and jump properly due to weakness in the core muscles of the body.[]

  • Polymyalgia Rheumatica

    METHODS: We studied 60 patients who had undergone 18 F-FDG PET/CT scans for workup of suspected PMR, arthritis, enthesitis, or myopathy.[] Gupta A, Thompson PD (2011) The relationship of vitamin D deficiency to statin myopathy. Atherosclerosis 215: 23–29. View Article Google Scholar 26.[] Phillips P, Haas R, Bannykh S, Hathaway S, Gray N, et al. (2002) Statin-associated myopathy with normal creatine kinase levels. Ann Intern Med 137: 581–585.[]

  • Limb-Girdle Muscular Dystrophy

    They are usually unable to stand without using their own body to steady themselves and, as such, present with Gower’s sign (where patients use their own hands to push off[] For this reason our finding extends the histological spectrum of myopathies due to ANO5 mutations as well as the possible differential diagnoses for necrotizing myopathy.[] In this report, a French family with an autosomal-dominant late-onset distal myopathy of the tibial muscular dystrophy phenotype segregating in several members of the family[]

  • Polymyositis

    Furthermore, glucocorticosteroid (GC) toxicity leads to a significant disability known as steroid myopathy, particularly in elderly patients.[] myopathies.[] We herein attempted to determine the features and etiologies of these myopathies.[]

  • Dermatomyositis

    Classification of the Autoimmune Myopathies. View Table Favorite Table Download (.pdf) Table 27–1. Classification of the Autoimmune Myopathies.[] BACKGROUND: Dermatomyositis (DM) is inflammatory myopathy or myositis characterized by muscle weakness and skin manifestations.[] The level of similarity between juvenile and adult myopathies regarding the presence of myositis-specific autoantibodies has not been fully elucidated.[]

  • Childhood Dermatomyositis

    Juvenile dermatomyositis, the most common inflammatory myopathy of childhood, is a rare systemic autoimmune vasculopathy that is characterised by weakness in proximal muscles[] […] enzyme defect, especially CCO deficiency is present not only in genetic disorders with mitochondrial involvement but in other neuromuscular disorders including inflammatory myopathies[] Inflammatory myopathies: Polymyositis, dermatomyositis, and related conditions.[]

  • Spinal Muscular Atrophy

    Children can sit without support but are unable to stand or walk unaided. Children also may have respiratory difficulties.[] Owing to the similar clinical features of SMA and congenital myopathy, an electrodiagnostic study and muscle biopsy could create confusion in the correct diagnosis in some[] They are able to sit without support but are unable to stand or walk unaided, and some may lose the ability to stay seated independently over time without treatment.[]

  • Muscular Atrophy

    […] to stand or walk.[] Children with SMA type II may eventually be able to sit, but they are unable to learn to stand or to walk.[] Summarizing what is known today, mutations in AIFM1 are associated with a progressive disorder with myopathy, ataxia and neuropathy.[]

  • Paraparesis

    I couldn’t stand longer than 20 minutes and I needed a cane to get around.[] Myopathies (inflammatory, toxic, inherited), neuromuscular junction disorders (botulism, myasthenia gravis), neuropathy (hereditary motor sensory neuropathy, alcohol, lead[] 45 HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis Is Not Associated with SNP rs12979860 of the IL-28B Gene. ( 26609200 ) 2015 46 Clinical presentation of axial myopathy[]

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