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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...
Autores principales: | Wakiguchi, Chiaki, Godai, Kohei, Mukaihara, Keika, Ohnou, Tetsuya, Kuniyoshi, Tamotsu, Masuda, Mina, Kanmura, Yuichi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
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 |
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