dc.contributor.author |
Peter, Appiah–Thompson |
|
dc.contributor.author |
Yaw, Asante Awuku |
|
dc.contributor.author |
Paul, Masiowsk |
|
dc.contributor.author |
Benedicta, L. Appiah–Thompson |
|
dc.contributor.author |
Dampson, Olukemi Olawaiye |
|
dc.date.accessioned |
2023-10-21T14:44:33Z |
|
dc.date.available |
2023-10-21T14:44:33Z |
|
dc.date.issued |
2015 |
|
dc.identifier.issn |
2231-0614 |
|
dc.identifier.uri |
http://hdl.handle.net/123456789/9827 |
|
dc.description.abstract |
ABSTRACT
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.iso |
en |
en_US |
dc.publisher |
British Journal of Medicine & Medical Research |
en_US |
dc.subject |
Myasthenia gravis; |
en_US |
dc.subject |
myasthenic crisis |
en_US |
dc.subject |
anti-MuSK |
en_US |
dc.subject |
puerperium. |
en_US |
dc.title |
Anti-musk Myasthenic Crisis in the Puerperium: The Management Dilemma |
en_US |
dc.type |
Article |
en_US |