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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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
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author Wakiguchi, Chiaki
Godai, Kohei
Mukaihara, Keika
Ohnou, Tetsuya
Kuniyoshi, Tamotsu
Masuda, Mina
Kanmura, Yuichi
author_facet Wakiguchi, Chiaki
Godai, Kohei
Mukaihara, Keika
Ohnou, Tetsuya
Kuniyoshi, Tamotsu
Masuda, Mina
Kanmura, Yuichi
author_sort Wakiguchi, Chiaki
collection PubMed
description 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 anesthesia. The child had an extremely low Bispectral Index (BIS) value prior to undergoing general anesthesia. Her perioperative course was uneventful. This case highlights some of the important anesthetic concerns in patients with MDS, which include potentially difficult airways and extremely low BIS values.
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spelling pubmed-58187032018-02-27 Management of general anesthesia in a child with Miller–Dieker syndrome: a case report Wakiguchi, Chiaki Godai, Kohei Mukaihara, Keika Ohnou, Tetsuya Kuniyoshi, Tamotsu Masuda, Mina Kanmura, Yuichi JA Clin Rep 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 anesthesia. The child had an extremely low Bispectral Index (BIS) value prior to undergoing general anesthesia. Her perioperative course was uneventful. This case highlights some of the important anesthetic concerns in patients with MDS, which include potentially difficult airways and extremely low BIS values. Springer Berlin Heidelberg 2015-09-18 2015 /pmc/articles/PMC5818703/ /pubmed/29497646 http://dx.doi.org/10.1186/s40981-015-0017-2 Text en © Wakiguchi et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Wakiguchi, Chiaki
Godai, Kohei
Mukaihara, Keika
Ohnou, Tetsuya
Kuniyoshi, Tamotsu
Masuda, Mina
Kanmura, Yuichi
Management of general anesthesia in a child with Miller–Dieker syndrome: a case report
title Management of general anesthesia in a child with Miller–Dieker syndrome: a case report
title_full Management of general anesthesia in a child with Miller–Dieker syndrome: a case report
title_fullStr Management of general anesthesia in a child with Miller–Dieker syndrome: a case report
title_full_unstemmed Management of general anesthesia in a child with Miller–Dieker syndrome: a case report
title_short Management of general anesthesia in a child with Miller–Dieker syndrome: a case report
title_sort management of general anesthesia in a child with miller–dieker syndrome: a case report
topic Case Report
url 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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