A Cohen syndrome patient whose muscle-relaxant effect may have been prolonged during general anesthesia: a case report

Cohen syndrome is a rare genetic disorder associated with mutations in the VPS13B gene. Individuals with this disorder present with diverse clinical manifestations, including muscle hypotonia, intellectual disabilities, and typical facial characteristics, such as prominent upper central incisors and...

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Detalles Bibliográficos
Autores principales: Ishikawa, Emi, Shibuya, Makiko, Kimura, Yukifumi, Kamekura, Nobuhito, Fujisawa, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dental Society of Anesthsiology 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995672/
https://www.ncbi.nlm.nih.gov/pubmed/35449785
http://dx.doi.org/10.17245/jdapm.2022.22.2.155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995672/
https://www.ncbi.nlm.nih.gov/pubmed/35449785
http://dx.doi.org/10.17245/jdapm.2022.22.2.155

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