COVID-19 in a Cohort of Patients with Congenital Myasthenic Syndrome

Author:

Alabaf Setareh12,O’Connell Karen1,Ramdas Sithara1,Beeson David12,Palace Jacqueline1

Affiliation:

1. Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK

2. Neurosciences Group, Weatherall Institute of Molecular Medicine, University of Oxford, The John Radcliffe Hospital, Oxford, UK

Abstract

Congenital Myasthenic Syndromes (CMS) are a rare group of genetic disorders of neuromuscular transmission. Some subtypes of CMS can be associated with respiratory and bulbar weakness and these patients may therefore be at high risk of developing a severe disease from COVID-19. We screened 73 patients with genetically confirmed CMS who were attending the UK national referral centre for evidence of previous Severe Acute Respiratory Syndrome Corona Virus 2 infection and their clinical outcome. Of 73 patients, seven had history of confirmed COVID-19. None of the infected patients developed a severe disease, and there were no signals that CMS alone carries a high risk of severe disease from COVID-19.

Publisher

IOS Press

Subject

Neurology (clinical),Neurology

Reference3 articles.

1. Inherited disorders of the neuromuscular junction: An update;Rodriguez Cruz;Journal of Neurology,2014

2. The congenital myasthenic syndromes;Palace;Journal of Neuroimmunology,2008

3. Favorable outcome of COVID-19 infection in a patient with congenital myasthenic syndrome;Bonanno;Neurological sciences: Official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology,2021

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