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Various authors have suggested that thyrotoxic myopathy is a result of the weight loss and generalized asthenia associated with hyperthyroidism. Muscle involvement has been reported to occur in about 80% of thyrotoxic patients (see section #Epidemiology ), [ 7 ] and the most common causes of hyperthyroidism are Graves’ disease , toxic ...
Lambert–Eaton syndrome, Eaton–Lambert syndrome, myasthenic syndrome, carcinomatous myopathy, cancer LEMS: Neuromuscular junction. Lambert–Eaton myasthenic syndrome is caused by autoantibodies to the presynaptic membrane. Myasthenia gravis is caused by autoantibodies to the postsynaptic acetylcholine receptors.
Distal muscular dystrophy, also called distal myopathy, is essentially any muscle disease that preferentially affects the hands and/or feet, a much less common pattern than proximal muscle weakness. Late adult-onset type 1; Late adult-onset type 2a; Late adult-onset type 2b; Early adult-onset type 1; Early adult-onset type 2; Early adult-onset ...
Thyrotoxic periodic paralysis (TPP) is a rare condition featuring attacks of muscle weakness in the presence of hyperthyroidism (overactivity of the thyroid gland). Hypokalemia (a decreased potassium level in the blood) is usually present during attacks.
NMT is a diverse disorder. As a result of muscular hyperactivity, patients may present with muscle cramps, stiffness, myotonia-like symptoms (slow relaxation), associated walking difficulties, hyperhidrosis (excessive sweating), myokymia (quivering of a muscle), fasciculations (muscle twitching), fatigue, exercise intolerance, myoclonic jerks and other related symptoms.
Pain control only necessitates symptomatic treatment with non-steroidal anti-inflammatory medications or aspirin. [2] Severely sick individuals may benefit from glucocorticoid medication, which often produces a substantial response in 24 to 48 hours. [4] Thyrotoxic symptoms are managed with beta-adrenergic blockers such atenolol and propranolol ...
Congenital nemaline myopathy (neuromuscular disorder) Specialty: Neurology, neuromuscular medicine, physical medicine and rehabilitation: Causes: Autoimmune disorders, [1] genetic disorders, [2] environmental factors [3] Diagnostic method: Muscle electrophysiology tests, genetic testing: Treatment: Depends on the disorder; many currently have ...
However, drugs most likely to impact myasthenic patients negatively are those used in the treatment of the disease. These include overuse of anticholinesterase drugs, high-dose prednisone, and anesthesia and neuromuscular blockers for thymectomy."(reference 39)