Anesthetic Approach to a Child with Noonan's Syndrome

Noonan syndrome is characterized by fascial and physical features along with congenital heart disease. In these patients, fascial features include short webbed neck, micrognathia, limited mouth opening and high arched palate. Pulmonary stenosis and hypertrophic obstructive cardiomyopathy are highly...

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Main Authors: Zehra Hatipoglu, Mediha Turktan, Ersel Gulec, Cagatay Kucukbingoz, Dilek Ozcengiz
Format: Article
Language:English
Published: Cukurova University 2015-03-01
Series:Çukurova Üniversitesi Tıp Fakültesi Dergisi
Subjects:
Online Access:http://www.scopemed.org/fulltextpdf.php?mno=182036
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spelling doaj-362ff3f536044e7687e20254cc00fd5b2020-11-24T21:47:20ZengCukurova UniversityÇukurova Üniversitesi Tıp Fakültesi Dergisi0250-51502015-03-014014750182036Anesthetic Approach to a Child with Noonan's SyndromeZehra Hatipoglu0Mediha Turktan1Ersel Gulec2Cagatay Kucukbingoz3Dilek Ozcengiz4Assist. Prof. Zehra Hatipoglu Cukurova University Faculty Of Medicine, Department of Anesthesiology and Reanimation, Adana Cukurova University Faculty Of Medicine, Department of Anesthesiology and Reanimation, Adana Cukurova University Faculty Of Medicine, Department of Anesthesiology and Reanimation, Adana/Turkey Cukurova University Faculty Of Medicine, Department of Anesthesiology and Reanimation, Adana/Turkey Cukurova University Faculty Of Medicine, Department of Anesthesiology and Reanimation, Adana/TurkeyNoonan syndrome is characterized by fascial and physical features along with congenital heart disease. In these patients, fascial features include short webbed neck, micrognathia, limited mouth opening and high arched palate. Pulmonary stenosis and hypertrophic obstructive cardiomyopathy are highly prevalent in Noonan's syndrome. The anesthetic management is important because of difficult airway and severe cardiac abnormalities. We reported that anesthetic management of a child with Noonan's syndrome. [Cukurova Med J 2015; 40(Suppl 1): 47-50]http://www.scopemed.org/fulltextpdf.php?mno=182036Noonan Syndromegeneral anesthesia
collection DOAJ
language English
format Article
sources DOAJ
author Zehra Hatipoglu
Mediha Turktan
Ersel Gulec
Cagatay Kucukbingoz
Dilek Ozcengiz
spellingShingle Zehra Hatipoglu
Mediha Turktan
Ersel Gulec
Cagatay Kucukbingoz
Dilek Ozcengiz
Anesthetic Approach to a Child with Noonan's Syndrome
Çukurova Üniversitesi Tıp Fakültesi Dergisi
Noonan Syndrome
general anesthesia
author_facet Zehra Hatipoglu
Mediha Turktan
Ersel Gulec
Cagatay Kucukbingoz
Dilek Ozcengiz
author_sort Zehra Hatipoglu
title Anesthetic Approach to a Child with Noonan's Syndrome
title_short Anesthetic Approach to a Child with Noonan's Syndrome
title_full Anesthetic Approach to a Child with Noonan's Syndrome
title_fullStr Anesthetic Approach to a Child with Noonan's Syndrome
title_full_unstemmed Anesthetic Approach to a Child with Noonan's Syndrome
title_sort anesthetic approach to a child with noonan's syndrome
publisher Cukurova University
series Çukurova Üniversitesi Tıp Fakültesi Dergisi
issn 0250-5150
publishDate 2015-03-01
description Noonan syndrome is characterized by fascial and physical features along with congenital heart disease. In these patients, fascial features include short webbed neck, micrognathia, limited mouth opening and high arched palate. Pulmonary stenosis and hypertrophic obstructive cardiomyopathy are highly prevalent in Noonan's syndrome. The anesthetic management is important because of difficult airway and severe cardiac abnormalities. We reported that anesthetic management of a child with Noonan's syndrome. [Cukurova Med J 2015; 40(Suppl 1): 47-50]
topic Noonan Syndrome
general anesthesia
url http://www.scopemed.org/fulltextpdf.php?mno=182036
work_keys_str_mv AT zehrahatipoglu anestheticapproachtoachildwithnoonanssyndrome
AT medihaturktan anestheticapproachtoachildwithnoonanssyndrome
AT erselgulec anestheticapproachtoachildwithnoonanssyndrome
AT cagataykucukbingoz anestheticapproachtoachildwithnoonanssyndrome
AT dilekozcengiz anestheticapproachtoachildwithnoonanssyndrome
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