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36 Possible Causes for Bilateral Pelvic Girdle Weakness

  • Polymyalgia Rheumatica

    This article is available to subscribers. Subscribe now . Already have an account? Sign in Clinical Practice Cornelia M. Weyand, M.D., Ph.D., and Jörg J. Goronzy, M.D., Ph.D. Article Figures/Media Metrics Both giant-cell arteritis and polymyalgia rheumatica are immune-mediated diseases that are treated with glucocorticoids,[…][doi.org]

  • Duchenne Muscular Dystrophy

    Open Access Review 1 Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, 44121 Italy 2 Bambino Gesù Hospital, Rome, 00146, Italy * Authors to whom correspondence should be addressed. Academic Editor: Leonidas A. Phylactou Received: 20 July 2015 / Revised: 15 September 2015 /[…][doi.org]

  • Erb Muscular Dystrophy

    Symptoms - Muscular dystrophy limb girdle type 2A- Erb type Muscle weakness is first evident in the shoulder girdle and later in the pelvic girdle.[checkorphan.org] The disability experienced by patients is fairly minimal, although frozen shoulder syndrome may significantly alter function if it is bilateral.[checkorphan.org]

  • Becker Muscular Dystrophy

    We previously reported a patient with Becker muscular dystrophy (BMD) who exhibited a benign clinical phenotype and marked expression of utrophin on the muscle cell membrane. The patient developed multiple episodes of thrombosis (middle cerebral and femoral arteries) in the course of the disease. We re-examined[…][ncbi.nlm.nih.gov]

  • Primary Hyperparathyroidism

    Recent data demonstrate decreased fracture risk after operation for asymptomatic primary hyperparathyroidism. We performed a revised cost-effectiveness analysis comparing parathyroidectomy versus observation while incorporating fracture risk reduction. A Markov transition-state model was created comparing[…][ncbi.nlm.nih.gov]

  • Oculopharyngeal Muscular Dystrophy

    Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of middle age presenting as progressive dysphagia and eyelid ptosis, due to short expansions of the GCG trinucleotide repeat (from GCG6 to GCG8-13) in the polyadenylate binding-protein nuclear 1 (PABPN1) gene. OPMD is rarely seen in Asians[…][ncbi.nlm.nih.gov]

  • Limb-Girdle Muscular Dystrophy

    PLoS One. 2013 Jun 28;8(6):e66929. doi: 10.1371/journal.pone.0066929. Print 2013. Author information 1 Neuromuscular Research Unit, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark. Abstract Patients with Limb girdle muscular dystrophy type 2I (LGMD2I) are characterized by[…][ncbi.nlm.nih.gov]

  • Inclusion Body Myositis

    Abstract Objectives: The study aimed to investigate the effects of a combined functional and aerobic exercise program on aerobic capacity, muscle strength, and functional mobility in a group of patients with sporadic inclusion body myositis (IBM). Methods: Aerobic capacity, muscle strength, and functional capacity[…][doi.org]

  • Steroid Myopathy

    Steroid myopathy is a condition characterized by weakness of the proximal muscles of the arms and legs and the flexor muscles of the neck. It can be caused by excessive endogenous or exogenous steroids and can be either acute in onset or chronic. Steroid myopathy (SM) was first described in 1932 by Cushing. It[…][symptoma.com]

  • Lambert Eaton Myasthenic Syndrome

    Lambert-Eaton myasthenic syndrome is a rare, but reasonably well-understood, antibody-mediated autoimmune disease that is caused by serum auto-antibodies and results in muscle weakness and autonomic dysfunction. One half of the patients have an idiopathic form, the other half a tumour-associated form of the[…][ncbi.nlm.nih.gov]

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