“Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis
Purpose: To report three cases of juvenile myasthenia gravis aged between 18 and 24 months with ocular symptoms as their first presentation. Method: A case series. Results: We present a case series of juvenile myasthenia gravis in a tertiary centre in Malaysia. Two of the three cases consist of a pa...
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my.um.eprints.288772022-04-21T04:35:51Z http://eprints.um.edu.my/28877/ “Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis Krishna, L. Abdul Jalil, N.F. Lott, P.W. Singh, S. Choo, M.M. RE Ophthalmology Purpose: To report three cases of juvenile myasthenia gravis aged between 18 and 24 months with ocular symptoms as their first presentation. Method: A case series. Results: We present a case series of juvenile myasthenia gravis in a tertiary centre in Malaysia. Two of the three cases consist of a pair of twins who presented with ptosis of bilateral eyes; the first twin presented 4 months later than the second twin. These two cases were positive for anti-acetylcholine receptor antibodies and had generalized myasthenia gravis, whereas the other case was negative for receptor antibodies and was purely ocular myasthenia gravis. Conclusion: Juvenile myasthenia gravis is relatively rare in toddlers. Early diagnosis and commencement of treatment is important to slow the progression of the disease and avoiding life-threatening events. © The Author(s) 2019. SAGE Publications 2021-03 Article PeerReviewed Krishna, L. and Abdul Jalil, N.F. and Lott, P.W. and Singh, S. and Choo, M.M. (2021) “Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis. European Journal of Ophthalmology, 31 (2). NP119-NP122. ISSN 1120-6721, DOI https://doi.org/10.1177/1120672119867605 <https://doi.org/10.1177/1120672119867605>. 10.1177/1120672119867605 |
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Purpose: To report three cases of juvenile myasthenia gravis aged between 18 and 24 months with ocular symptoms as their first presentation. Method: A case series. Results: We present a case series of juvenile myasthenia gravis in a tertiary centre in Malaysia. Two of the three cases consist of a pair of twins who presented with ptosis of bilateral eyes; the first twin presented 4 months later than the second twin. These two cases were positive for anti-acetylcholine receptor antibodies and had generalized myasthenia gravis, whereas the other case was negative for receptor antibodies and was purely ocular myasthenia gravis. Conclusion: Juvenile myasthenia gravis is relatively rare in toddlers. Early diagnosis and commencement of treatment is important to slow the progression of the disease and avoiding life-threatening events. © The Author(s) 2019. |
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Article |
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Krishna, L. Abdul Jalil, N.F. Lott, P.W. Singh, S. Choo, M.M. |
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Krishna, L. Abdul Jalil, N.F. Lott, P.W. Singh, S. Choo, M.M. |
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Krishna, L. |
title |
“Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis |
title_short |
“Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis |
title_full |
“Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis |
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“Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis |
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“Mummy, my eyelids are heavy”: A case series of juvenile myasthenia gravis |
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“mummy, my eyelids are heavy”: a case series of juvenile myasthenia gravis |
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SAGE Publications |
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2021 |
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http://eprints.um.edu.my/28877/ |
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