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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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Bibliografiska uppgifter
I publikationen:JA Clin Rep
Huvudupphovsmän: Wakiguchi, Chiaki, Godai, Kohei, Mukaihara, Keika, Ohnou, Tetsuya, Kuniyoshi, Tamotsu, Masuda, Mina, Kanmura, Yuichi
Materialtyp: Artigo
Språk:Inglês
Publicerad: Springer Berlin Heidelberg 2015
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5818703/
https://ncbi.nlm.nih.gov/pubmed/29497646
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40981-015-0017-2
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