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Hereditary pseudocholinesterase deficiency discovery after electroconvulsive therapy
Inherited pseudocholinesterase deficiency refers to an uncommon defect in the butyrylcholinesterase enzyme which can result in prolonged muscle paralysis due to delayed breakdown of choline ester paralytic anaesthetic agents. We describe a 25-year-old woman receiving electroconvulsive therapy (ECT)...
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| Publicado no: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7813341/ https://ncbi.nlm.nih.gov/pubmed/33462045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-239206 |
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