Prepubertal Juvenile Myasthenia Gravis; A Case With Early Onset And Bulbar Symptoms

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dc.contributor.authorEkmekci, Ozgul
dc.contributor.authorKarasoy, Hatice
dc.date.accessioned2019-10-27T21:53:46Z
dc.date.available2019-10-27T21:53:46Z
dc.date.issued2013
dc.departmentEge Üniversitesien_US
dc.description.abstractJuvenile myasthenia gravis (JMG) is a rare autoimmune disease affecting the neuromuscular junction in children and adolescents. Its clinical presentation is usually associated with ethnicity and pubertal development. We present a 14 month old patient with, bulbar symptoms and a good clinical course. The age of onset in this case is lower than average and the case is in pharmacological remission after medical treatment. Prepubertal JMG is very rare during infancy in Caucasians and ocular symptoms are more common in prepubertal patients. This Caucasian case is uncommon since she has presented with bulbar symptoms and early onset.en_US
dc.identifier.endpage586en_US
dc.identifier.issn1302-1664
dc.identifier.issn1302-1664en_US
dc.identifier.issue3en_US
dc.identifier.startpage583en_US
dc.identifier.urihttps://hdl.handle.net/11454/47961
dc.identifier.volume30en_US
dc.identifier.wosWOS:000328090600014en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherJournal Neurological Sciencesen_US
dc.relation.ispartofJournal of Neurological Sciences-Turkishen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectJuvenile myasthenia gravisen_US
dc.subjectneuromuscular junctionen_US
dc.subjectautoimmune diseaseen_US
dc.titlePrepubertal Juvenile Myasthenia Gravis; A Case With Early Onset And Bulbar Symptomsen_US
dc.typeArticleen_US

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