Clinical and biochemical footprints of inherited metabolic diseases: I. Movement disorders

About a third of patients with inherited metabolic diseases with neurologic involvement suffer from a movement disorder, in the form of ataxia, hyperkinetic movements, or hypokinetic-rigid syndrome. We reviewed and updated the list of known metabolic etiologies associated with various types of movem...

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Hauptverfasser: Ferreira Lopez, Carlos R (VerfasserIn) , Hoffmann, Georg F. (VerfasserIn) , Blau, Nenad (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 26 March 2019
In: Molecular genetics and metabolism
Year: 2019, Jahrgang: 127, Heft: 1, Pages: 28-30
ISSN:1096-7206
DOI:10.1016/j.ymgme.2019.03.007
Online-Zugang:Verlag, Volltext: https://doi.org/10.1016/j.ymgme.2019.03.007
Verlag: http://www.sciencedirect.com/science/article/pii/S109671921830739X
Volltext
Verfasserangaben:Carlos R. Ferreira, Georg F. Hoffmann, Nenad Blau

MARC

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520 |a About a third of patients with inherited metabolic diseases with neurologic involvement suffer from a movement disorder, in the form of ataxia, hyperkinetic movements, or hypokinetic-rigid syndrome. We reviewed and updated the list of known metabolic etiologies associated with various types of movement disorders, and found approximately 200 relevant inborn errors of metabolism. This represents the first of a series of articles attempting to create and maintain a comprehensive list of clinical and metabolic differential diagnoses according to system involvement. 
650 4 |a Ataxia 
650 4 |a Choreoathetosis 
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