Sedation with 4-hydroxybutyric acid: A potential pitfall in the diagnosis of SSADH deficiency

9Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

Deficiency of succinic semialdehyde dehydrogenase (SSADH) is a rare neurometabolic disorder with accumulation of 4-hydroxybutyric acid (4-HBA) as a biochemical hallmark. We present a boy with an unresolved severe neurological disorder and intermittent elevation of 4-HBA in serum and CSF which was later shown to result from iatrogenic administration of 4-HBA for sedation purposes. © SSIEM and Kluwer Academic Publishers.

Cite

CITATION STYLE

APA

Wolf, N. I., Haas, D., Hoffmann, G. F., Jakobs, C., Salomons, G. S., Wevers, R. A., … Rating, D. (2004). Sedation with 4-hydroxybutyric acid: A potential pitfall in the diagnosis of SSADH deficiency. Journal of Inherited Metabolic Disease, 27(2), 291–293. https://doi.org/10.1023/B:BOLI.0000028842.15981.6e

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free