Myasthenia gravis.

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dc.contributor.authorAnandam, Ren_US
dc.date.accessioned1989-03-01en_US
dc.date.accessioned2009-05-30T11:25:52Z
dc.date.available1989-03-01en_US
dc.date.available2009-05-30T11:25:52Z
dc.date.issued1989-03-01en_US
dc.description.abstractTwelve children with myasthenic symptoms were seen over a period of 6 years. The age of onset of symptoms ranged from 6 months to 9 years. On followup for a mean period of 4.25 years, (longest followup was 9 years) five children went into complete remission of symptoms after treatment with prostigmine; three children responded to prostigmine and steroids; two children were relieved of symptoms without prolonged treatment and the remaining two children could not be followed up. Thymectomy was not advised in any patient.en_US
dc.identifier.citationAnandam R. Myasthenia gravis. Indian Journal of Pediatrics. 1989 Mar-Apr; 56(2): 277-82en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/79667
dc.language.isoengen_US
dc.source.urihttps://medind.nic.in/icb/icbai.shtmlen_US
dc.subject.meshChilden_US
dc.subject.meshChild, Preschoolen_US
dc.subject.meshFemaleen_US
dc.subject.meshFollow-Up Studiesen_US
dc.subject.meshGlucocorticoids --therapeutic useen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshMaleen_US
dc.subject.meshMyasthenia Gravis --congenitalen_US
dc.subject.meshNeostigmine --therapeutic useen_US
dc.subject.meshRemission Inductionen_US
dc.titleMyasthenia gravis.en_US
dc.typeJournal Articleen_US
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