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Congenital myasthenia gravis
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2013; 23 (7): 517-518
de En | IMEMR | ID: emr-147505
Bibliothèque responsable: EMRO
Congenital myasthenia gravis is caused by genetic mutations affecting neuromuscular transmission, characterized by muscle weakness usually starting in childhood. A two and a half years old male child presented with bilateral ptosis and hoarseness of voice. The symptoms progressed giving the clinical impression of congenital myasthenia gravis. A series of tests were done including Ice Pack Test, acetylcholine receptor antibody test, trial of steroids and finally neostigmine test which confirmed the diagnosis. This case illustrates the challenges in diagnosing congenital myasthenia gravis and highlights the potential benefits of neostigmine test in its diagnosis
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Indice: IMEMR langue: En Texte intégral: J. Coll. Physicians Surg. Pak. Année: 2013
Recherche sur Google
Indice: IMEMR langue: En Texte intégral: J. Coll. Physicians Surg. Pak. Année: 2013