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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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| Veröffentlicht in: | BMJ Case Rep |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
2021
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| Schlagworte: | |
| Online Zugang: | 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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