Familial infantile myaesthenia.
dc.contributor.author | Bhaskaran, R | en_US |
dc.contributor.author | Ravikumar, A | en_US |
dc.contributor.author | Prakash, M | en_US |
dc.contributor.author | Eapen, S | en_US |
dc.date.accessioned | 2000-04-29 | en_US |
dc.date.accessioned | 2009-05-30T21:48:36Z | |
dc.date.available | 2000-04-29 | en_US |
dc.date.available | 2009-05-30T21:48:36Z | |
dc.date.issued | 2000-04-29 | en_US |
dc.description.abstract | We report a family of two brothers with familial infantile myaesthenia which is an autosomal recessive congenital myaesthenic syndrome. It is a presynaptic neuro muscular junction disorder, responsive to treatment and has got good prognosis. | en_US |
dc.description.affiliation | Department of Neurology, Medical College Hospital, Thiruvananthapuram. | en_US |
dc.identifier.citation | Bhaskaran R, Ravikumar A, Prakash M, Eapen S. Familial infantile myaesthenia. Journal of the Association of Physicians of India. 2000 Apr; 48(4): 439-40 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/88958 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://www.japi.org | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Cholinesterase Inhibitors --therapeutic use | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Myasthenic Syndromes, Congenital --drug therapy | en_US |
dc.title | Familial infantile myaesthenia. | en_US |
dc.type | Case Reports | en_US |
dc.type | Journal Article | en_US |
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