Management of general anesthesia in a child with Miller–Dieker syndrome: a case report

Miller–Dieker syndrome (MDS) is a rare disorder characterized by type I lissencephaly and a distinctive facial appearance that may include prominent forehead, bitemporal hollowing, and micrognathia. MDS is associated with epilepsy. We here report an 18-month-old girl with MDS who required general an...

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Detalles Bibliográficos
Autores principales: Wakiguchi, Chiaki, Godai, Kohei, Mukaihara, Keika, Ohnou, Tetsuya, Kuniyoshi, Tamotsu, Masuda, Mina, Kanmura, Yuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818703/
https://www.ncbi.nlm.nih.gov/pubmed/29497646
http://dx.doi.org/10.1186/s40981-015-0017-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818703/
https://www.ncbi.nlm.nih.gov/pubmed/29497646
http://dx.doi.org/10.1186/s40981-015-0017-2

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