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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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| I publikationen: | JA Clin Rep |
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| Huvudupphovsmän: | , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Springer Berlin Heidelberg
2015
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| 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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