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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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| Publicat a: | BMJ Case Rep |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
2021
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| Matèries: | |
| Accés en línia: | 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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