Cerebellar hypometabolism with normal structural findings in Cerebrotendinous xanthomatosis. A case report

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Cerebellar hypometabolism with normal structural findings in Cerebrotendinous xanthomatosis. A case report

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作者：Michele Ragno^a ; Fabio Di Marzio^a ; Chiara Fuccio^b ; Luigi Pianese^c ; Valeria Cozzolino^c ; Terenzio Carboni^a ; Antonio Cinti^a ; Giordano D&rsquo ; Andreamatteo^a ; Luigi Trojano^d ; ^{luigi.trojano@unina2.it" class="auth_mail" title="E-mail the corresponding author} ; Andrea Mignarri^e ; Gian Nicola Gallus^e ; Maria Teresa Dotti^e
关键词：Cerebrotendinous xanthomatosis ; Autosomal recessive disorder ; Spastic paraparesis ; 18FDG PET ; Cerebellum
刊名：Clinical Neurology and Neurosurgery
出版年：2015
出版时间：December 2015
年：2015
卷：139
期：Complete
页码：221-223
全文大小：378 K

文摘

•: In Cerebrotendinous xanthomatosis spastic paraparesis is the most common motor sign.
•: 18FDG PET can reveal functional impairments preceding brain anatomic alterations.
•: 18FDG PET may be useful to detect dentate dysfunction when CTX is clinically suspected.

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