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Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)

Frontometaphyseal dysplasia (FMD), also called Gorlin-Cohen syndrome, is a rare hereditary X-linked dominant craniotubular bone disorder. The presentation describes the airway management of a 2-year-old child suffering from FMD with significant retrognathia, posted for major long bone corrective ost...

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Autores principales: Ganigara, Anuradha, Nishtala, Madhavi, Chandrika, Yabagodu Rama Vakoda, Chandrakala, Kunigal Ravishankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009657/
https://www.ncbi.nlm.nih.gov/pubmed/24803775
http://dx.doi.org/10.4103/0970-9185.130100
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author Ganigara, Anuradha
Nishtala, Madhavi
Chandrika, Yabagodu Rama Vakoda
Chandrakala, Kunigal Ravishankar
author_facet Ganigara, Anuradha
Nishtala, Madhavi
Chandrika, Yabagodu Rama Vakoda
Chandrakala, Kunigal Ravishankar
author_sort Ganigara, Anuradha
collection PubMed
description Frontometaphyseal dysplasia (FMD), also called Gorlin-Cohen syndrome, is a rare hereditary X-linked dominant craniotubular bone disorder. The presentation describes the airway management of a 2-year-old child suffering from FMD with significant retrognathia, posted for major long bone corrective osteotomy. Induction with a combination of dexmedetomidine and ketamine preceded a successful endotracheal intubation under spontaneous ventilation.
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spelling pubmed-40096572014-05-06 Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome) Ganigara, Anuradha Nishtala, Madhavi Chandrika, Yabagodu Rama Vakoda Chandrakala, Kunigal Ravishankar J Anaesthesiol Clin Pharmacol Case Report Frontometaphyseal dysplasia (FMD), also called Gorlin-Cohen syndrome, is a rare hereditary X-linked dominant craniotubular bone disorder. The presentation describes the airway management of a 2-year-old child suffering from FMD with significant retrognathia, posted for major long bone corrective osteotomy. Induction with a combination of dexmedetomidine and ketamine preceded a successful endotracheal intubation under spontaneous ventilation. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4009657/ /pubmed/24803775 http://dx.doi.org/10.4103/0970-9185.130100 Text en Copyright: © Journal of Anaesthesiology Clinical Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ganigara, Anuradha
Nishtala, Madhavi
Chandrika, Yabagodu Rama Vakoda
Chandrakala, Kunigal Ravishankar
Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)
title Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)
title_full Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)
title_fullStr Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)
title_full_unstemmed Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)
title_short Airway management of a child with frontometaphyseal dysplasia (Gorlin Cohen syndrome)
title_sort airway management of a child with frontometaphyseal dysplasia (gorlin cohen syndrome)
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009657/
https://www.ncbi.nlm.nih.gov/pubmed/24803775
http://dx.doi.org/10.4103/0970-9185.130100
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