Case Report
Congenital Myasthenia Gravis: A Case Report
Bhramara Madduri1*, Seemantini Ayachit2, Milena Dimic3, Praveen Kumar4 and Neeta Raju5
1Department of Pediatrics and Neonatology, Royal Bahrain hospital, Bahrain
2Fellowship Pediatric Ophthalmology, Royal Bahrain hospital, Bahrain
3Department of Pediatric Neurologist, Royal Bahrain Hospital, Bahrain
4Fellowship Pediatric Neurology, Royal Bahrain hospital, Bahrain
5Department of Pediatrics, Royal Bahrain hospital, Bahrain
Bhramara Madduri, Department of Pediatrics and Neonatology, Royal Bahrain hospital, Bahrain.
Received Date: November 01, 2020; Published Date: November 16, 2020
Abstract
Congenital myasthenia gravis (CMS) is not very uncommon but could be easily missed. Timely identification and management can improve quality of life. Here we present a case of congenital myasthenia gravis, confirmed by genetic studies, detected at 2 years of age.
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Bhramara Madduri, Seemantini Ayachit, Milena Dimic, Praveen Kumar, Neeta Raju. Congenital Myasthenia Gravis: A Case Report. Glob J of Ped & Neonatol Car. 3(1): 2020. GJPNC.MS.ID.000553.