Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/9827
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dc.contributor.authorPeter, Appiah–Thompson-
dc.contributor.authorYaw, Asante Awuku-
dc.contributor.authorPaul, Masiowsk-
dc.contributor.authorBenedicta, L. Appiah–Thompson-
dc.contributor.authorDampson, Olukemi Olawaiye-
dc.date.accessioned2023-10-21T14:44:33Z-
dc.date.available2023-10-21T14:44:33Z-
dc.date.issued2015-
dc.identifier.issn2231-0614-
dc.identifier.urihttp://hdl.handle.net/123456789/9827-
dc.description.abstractABSTRACT Myasthenia gravis (MG) is a chronic neuromuscular junction (NMJ) dysfunction with a wide spectrum of neurological manifestations. MG is as a result of autoantibodies directed against NMJ at the postsynaptic level involving nicotinic or other postsynaptic antigens. The newly identified subtype of MG with antibodies against the muscle-specific receptor tyrosine kinase (Anti-MuSK) shows an unpredictable response to current MG treatment. The initial presentation of this disease entity often poses a diagnostic challenge and a treatment dilemma to the clinician. We present a case of life threatening Anti-MuSK-positive myasthenic crisis occurring during puerperium which required a temporary surgical airway and percutaneous endoscopic gastrostomy tube for feeding. She had dysphonia for 7 years but was not diagnosed. The complications and management dilemma of this case report are highlighted.en_US
dc.language.isoenen_US
dc.publisherBritish Journal of Medicine & Medical Researchen_US
dc.subjectMyasthenia gravis;en_US
dc.subjectmyasthenic crisisen_US
dc.subjectanti-MuSKen_US
dc.subjectpuerperium.en_US
dc.titleAnti-musk Myasthenic Crisis in the Puerperium: The Management Dilemmaen_US
dc.typeArticleen_US
Appears in Collections:School of Medical Sciences

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