Cholinesterase Deficiency Syndrome—A Pitfall in the Use of Butyrylcholinesterase as a Biomarker for Wilson’s Disease

A family is described as having two recessively inherited metabolic diseases and three differently affected children. During the explantation of a drain tube grommet under general anesthesia, a prolonged resuscitation and wake-up period occurred in the key case when he was 8 years old. This led to a...

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Detalles Bibliográficos
Autores principales: Arslan, Max, Novak, Max, Rosenthal, Dietmar, Hartmann, Christian J., Albrecht, Philipp, Samadzadeh, Sara, Hefter, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599139/
https://www.ncbi.nlm.nih.gov/pubmed/36291607
http://dx.doi.org/10.3390/biom12101398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599139/
https://www.ncbi.nlm.nih.gov/pubmed/36291607
http://dx.doi.org/10.3390/biom12101398

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