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cornelia de lange

Link: Severe complication of catatonia in a young patient with Hashimoto’s encephalopathy comorbid with Cornelia de Lange syndrome

Dear Editor,

Cornelia de Lange syndrome (CdLs) is a rare genetic disease diagnosed as a cluster of symptoms; however, there are only a few reports mentioning the immunologic problems in patients with CdLs. Hashimoto’s encephalopathy (HE) is an autoimmune encephalitis, which manifests as neurocognitive impairment and elevated antithyroid antibody (ATA) titers. Childhood HE manifests especially as more neuropsychiatric symptoms. However, there are no reports discussing the most severe neuropsychiatric complication, that is, catatonia, in HE. We herein report the first case of a severe complication of catatonia in a patient with HE comorbid with CdLs.

The full text of this “letter to the editor” published in Kaohsiung Journal of Medical Sciences can be found at http://www.kjms-online.com/article/S1607-551X(14)00142-9/fulltext.

Copyright © 2014 Published by Elsevier Inc. | by Yen-Wen Chen, Pi-Lien Hung, Ching-Kuan Wu, and Ping-Tao Tseng

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This website is not a substitute for independent professional advice. Nothing contained in this site is intended to be used as medical advice. No articles, personal accounts, or other content are intended to be used to diagnose, treat, cure or prevent any disease, nor should it be used for therapeutic purposes or as a substitute for your own health professionals advice.