Myasthenia Gravis
รหัสดีโอไอ
Creator Winita Fowsantear
Title Myasthenia Gravis
Contributor Sutthiwan Thammawat, Jinatta Jittiwat
Publisher Faculty of Pharmaceutical Sciences KKU MSU UBU
Publication Year 2561
Journal Title Isan Journal of Pharmaceutical Sciences
Journal Vol. 14
Journal No. 2
Page no. 16-25
Keyword Myasthenia gravis, autoimmune disease, neuromuscular junction, autoantibody, nicotinic acetylcholine receptor, acetylcholine
URL Website https://tci-thaijo.org/index.php/IJPS
Website title Isan Journal ofPharmaceutical Sciences, IJPS
ISSN 19050852
Abstract Myasthenia gravis (MG) is an autoimmune disease that affects the neuromuscular junction. In Thailand, MG affects approximately 2.17 patients per 100,000 population. MG is primary caused by autoantibodies directing towards the nicotinic acetylcholine receptors at the post synaptic membrane leading to muscle weakness. The clinical characteristic signs and symptoms of myasthenia gravis are ptosis, diplopia, weakness in chewing, difficult in swallowing and fluctuating levels of skeletal muscle weakness. The severity of weakness and fatigability fluctuates during the day, usually being least severe in the morning and worse as the day progress, especially during exercise or continuous repetitive motion with at least partially restored strength after period of rest. There are two approaches for management of MG based on the pathophysiology of this disease. The first treatment is by increasing the amount of acetylcholine that is available to bind with the nicotinic acetylcholine receptor at postsynaptic membrane using an acetylcholinesterase inhibitor agent. The second approach is by using immunosuppressive medications that can reduce the binding of nicotinic acetylcholine receptors by antibodies.
Faculty of Pharmaceutical Sciences, Khon Kaen University

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