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This Concept Map, created with IHMC CmapTools, has information related to: NMJ_myositis_muscular dystrophies, abnormal epxression of myotonin protein kinase gets worse with every generation, perimysial inflammation and atrophy CD4+T cells (humeral mediated B cell) increased cretaine kinase & anti-Jo-1, endomysial inflammation with CD8+T cells treatment steroids oral prednisone, Muscular dystrophies Congenital autosommal recessive muscular weakness early infancy without Brain malformation, Muscular dystrophies Congenital autosommal recessive muscular weakness early infancy with Brain malformation, metaplasia of skeletal muscle following muscle trauma More gradual onset!! caused endomysial inflammation with CD8+T cells, Myasthenia Gravis clinical presentation Ptosis, diplopia weakness worsens with muscle use, merosin (laminin 2) clinical signs non-progressive profound muscle weakness and doesn't walk independently, accelerated muscle breakdown primarily affects proximal muscles, Muscle weakness perception of weakness get more history, perimysial inflammation and atrophy CD4+T cells (humeral mediated B cell) treatment steroids oral prednisone, Lambert-Eaton myasthenic syndrome clinical presentation proximal muscle weakness autonomic symptoms (dry mouth, impotence) & improves with muscle use, Fragile X repeated CGG ????, Fukuyama congenital MD Muscle-eye brain disease Walker warburg abnormal glycosylation of alpha-dystroglycan, endomysial inflammation with CD8+T cells increased cretaine kinase & anti-Jo-1, proximal muscle weakness autonomic symptoms (dry mouth, impotence) & improves with muscle use treatment AChE minimal effect Remove tumor treat with prednisone, muscular abnormalities types Neuromuscular junction disease, Neuromuscular junction disease autoantibodies to presynaptic Ca channels dec. ACh release Lambert-Eaton myasthenic syndrome, Neuromuscular junction disease Most common Myasthenia Gravis, with Brain malformation types Fukuyama congenital MD Muscle-eye brain disease Walker warburg