Acute dystonia in a patient with 22q11.2 deletion syndrome

The 22q11.2 deletion syndrome (di George syndrome) is one of the most prevalent genetic disorders. The clinical features of the syndrome are distinct facial appearance, velopharyngeal insufficiency, conotruncal heart disease, parathyroid and immune dysfunction; however, little is known about possibl...

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Bibliographic Details
Main Authors: Konstantinos Kontoangelos, Antonis Maillis, Maria Maltezou, Sofia Tsiori, Charalambos C. Papageorgiou
Format: Article
Language:English
Published: Wiley 2015-09-01
Series:Mental Illness
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Online Access:http://www.pagepress.org/journals/index.php/mi/article/view/5902
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