학술논문
A Rare Neurological Presentation of Noonan Syndrome and Its Management—A Case Report.
Document Type
Case Study
Source
Subject
*NOONAN syndrome
*CONGENITAL heart disease
*CRANIOVERTEBRAL junction
*CONGENITAL disorders
*CEREBROVASCULAR disease
*
*
*
*
Language
ISSN
1793-5482
Abstract
Although Noonan syndrome is a relatively common congenital disorder with autosomal dominant inheritance, its association with cerebrovascular anomalies is rare. We report a case of a 20-year-old with Noonan syndrome with cerebrovascular aneurysm, who underwent successful endovascular coiling. Only four cases of cerebrovascular aneurysms in Noonan syndrome have been reported in the literature so far. To the best of our knowledge, this is only the fifth reported case and the first one that has been treated successfully with endovascular coiling. We hereby discuss the management of this case, which had several comorbidities like congenital heart disease and craniovertebral junction anomaly. [ABSTRACT FROM AUTHOR]