Noonan Syndrome and Stroke: A Case Report

Noonan syndrome is an autosomal dominant genetic disease characterized by short stature, webbed neck, typical facial appearance and congenital heart disease. Here we report a 24 year old woman patient with the diagnosis of Noonan syndrome who admitted to our clinic with ischemic stroke caused by atr...

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Main Authors: Ebru Nur Mıhçı, Murat Uçak, Ercan Mıhçı, Berrin Aktekin
Format: Article
Language:English
Published: Galenos Yayinevi 2012-03-01
Series:Türk Nöroloji Dergisi
Subjects:
Online Access:http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-59023&look4=
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spelling doaj-3cf06adadaf34ef08c9f3001f4ada9c12021-09-02T18:35:28ZengGalenos YayineviTürk Nöroloji Dergisi1301-062X2012-03-01181363810.4274/Tnd.59023Noonan Syndrome and Stroke: A Case ReportEbru Nur Mıhçı0Murat Uçak1Ercan Mıhçı2Berrin Aktekin3Department Of Neurology, Akdeniz University Faculty Of Medicine, Antalya, TurkeyDepartment Of Neurology, Akdeniz University Faculty Of Medicine, Antalya, TurkeyDepartment Of Pediatric Genetic, Akdeniz University Faculty Of Medicine, Antalya, TurkeyDepartment Of Neurology, Akdeniz University Faculty Of Medicine, Antalya, TurkeyNoonan syndrome is an autosomal dominant genetic disease characterized by short stature, webbed neck, typical facial appearance and congenital heart disease. Here we report a 24 year old woman patient with the diagnosis of Noonan syndrome who admitted to our clinic with ischemic stroke caused by atrial fibrillation secondary to hypertrophic cardiomyopathy. Noonan syndrome patients with stroke due to vascular malformations have been reported, but non-obstructive hypertrophic cardiomyopathy is a rare cause for stroke in patients with Noonan syndrome. Our aim of presenting the case emphasize that Noonan syndrome should be thought as a differential diagnosis in patients with stroke at a young age and dysmorphic facial appearance.http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-59023&look4=Noonan syndromeischemic strokevascular malformations
collection DOAJ
language English
format Article
sources DOAJ
author Ebru Nur Mıhçı
Murat Uçak
Ercan Mıhçı
Berrin Aktekin
spellingShingle Ebru Nur Mıhçı
Murat Uçak
Ercan Mıhçı
Berrin Aktekin
Noonan Syndrome and Stroke: A Case Report
Türk Nöroloji Dergisi
Noonan syndrome
ischemic stroke
vascular malformations
author_facet Ebru Nur Mıhçı
Murat Uçak
Ercan Mıhçı
Berrin Aktekin
author_sort Ebru Nur Mıhçı
title Noonan Syndrome and Stroke: A Case Report
title_short Noonan Syndrome and Stroke: A Case Report
title_full Noonan Syndrome and Stroke: A Case Report
title_fullStr Noonan Syndrome and Stroke: A Case Report
title_full_unstemmed Noonan Syndrome and Stroke: A Case Report
title_sort noonan syndrome and stroke: a case report
publisher Galenos Yayinevi
series Türk Nöroloji Dergisi
issn 1301-062X
publishDate 2012-03-01
description Noonan syndrome is an autosomal dominant genetic disease characterized by short stature, webbed neck, typical facial appearance and congenital heart disease. Here we report a 24 year old woman patient with the diagnosis of Noonan syndrome who admitted to our clinic with ischemic stroke caused by atrial fibrillation secondary to hypertrophic cardiomyopathy. Noonan syndrome patients with stroke due to vascular malformations have been reported, but non-obstructive hypertrophic cardiomyopathy is a rare cause for stroke in patients with Noonan syndrome. Our aim of presenting the case emphasize that Noonan syndrome should be thought as a differential diagnosis in patients with stroke at a young age and dysmorphic facial appearance.
topic Noonan syndrome
ischemic stroke
vascular malformations
url http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-59023&look4=
work_keys_str_mv AT ebrunurmıhcı noonansyndromeandstrokeacasereport
AT muratucak noonansyndromeandstrokeacasereport
AT ercanmıhcı noonansyndromeandstrokeacasereport
AT berrinaktekin noonansyndromeandstrokeacasereport
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