Open Access 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

Corresponding Author

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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