2012
DOI: 10.1016/j.neurol.2011.07.017
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Seronegative myasthenia gravis with bladder dysfunction

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Cited by 4 publications
(4 citation statements)
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“…Among the few existing studies, Dixon et al [ 10 ] reported cases of stress urinary incontinence in limb-girdle muscular dystrophy and Dickson et al [ 11 ] reported cases of myotonic dystrophy, both likely due to pelvic floor weakness. In MG, a variety of LUTS have been reported in case reports, from overactive bladder and urinary incontinence [ 2 , 3 ] to retention [ 4 ] (Table 3 ). However, it remains uncertain to what extent MG contributes to the LUTS.…”
Section: Discussionmentioning
confidence: 99%
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“…Among the few existing studies, Dixon et al [ 10 ] reported cases of stress urinary incontinence in limb-girdle muscular dystrophy and Dickson et al [ 11 ] reported cases of myotonic dystrophy, both likely due to pelvic floor weakness. In MG, a variety of LUTS have been reported in case reports, from overactive bladder and urinary incontinence [ 2 , 3 ] to retention [ 4 ] (Table 3 ). However, it remains uncertain to what extent MG contributes to the LUTS.…”
Section: Discussionmentioning
confidence: 99%
“…Although the muscles directly associated with the lower urinary tract (LUT) are smooth muscles, they are further surrounded by the striated muscles of the external sphincter and the pelvic floor. LUT symptoms (LUTSs) have been reported in case reports of MG, varying from overactive bladder and urinary incontinence [ 2 , 3 ] to retention [ 4 ]. However, it remains uncertain to what extent MG pathology contributes to the LUTS.…”
Section: Introductionmentioning
confidence: 99%
“…18 Marouani et al retained bladder dysfunction with urethral sphincter hypertonia and detrusor areflexia in a myasthenic girl. 19 On the other hand, Pannek and Grigoleit reported a 6-year-old boy who had congenital MG and suffered from OAB starting after initiating pyridostigmine and improving through functional electrical stimulation. 20 Likewise, Antoniou et al recovered urodynamic detrusor overactivity by using pretibial nerve stimulation in a young myasthenic woman.…”
Section: Discussionmentioning
confidence: 99%
“…After reviewing existing criteria for seronegative MG classification in dogs, we strongly believe the dog described here had seronegative MG, because of the clinical signs consistent with MG, positive edrophonium response, decremental response of the compound muscle action potential, and normalization of limb muscle weakness after anticholinesterase treatment. In humans, dysuria occurs in myasthenic patients, and there is also evidence for this in dogs , . It has been hypothesized that this is because of autoantibodies directed against ganglionic acetylcholine receptors in the autonomic nervous system .…”
Section: Discussionmentioning
confidence: 99%