Neurol. praxi. 2022;23(2):108-112 | DOI: 10.36290/neu.2021.082

Treatable inherited metabolic disorders with extrapyramidal manifestation in children

doc. MUDr. Miriam Kolníková, PhD., MUDr. Dominika Kovárová, MUDr. Patrícia Balážová, MUDr. Silvia Radová

Klinika detskej neurológie LF UK a NÚDCH, Bratislava

Inherited metabolic disorders are often manifested by movement disorders that are more or less expressed in the clinical presentation. They can be hyperkinetic: dystonia, chorea, athetosis, myoclonus, tremor stereotypies or hypokinetic: hypokinetic-rigid syndrome. Diagnosis of these diseases is often very difficult, because of the fact that the same movement disorder can be caused by various diseases. To our current knowledge, more than two hundred inherited metabolic disorders associated with movement disorders have been registered so far. In half of these diseases two or more symptoms are present, the most common of which are ataxia and dystonia. Appropriate diagnostic approach, which requires an accurate description of movement disorder, is impor­tant for early diagnosis and treatment (type, age and character of onset, extent of onset) as well as other neurological and others symptoms, laboratory results, radiological findings, genetic testing. The essential goal is rapid detection of treatable disorders.

Keywords: inherited metabolic disorders, dystonia, chorea, athetosis, hypokinetic-rigid syndrome.

Received: September 27, 2021; Revised: October 18, 2021; Accepted: October 18, 2021; Prepublished online: October 18, 2021; Published: April 21, 2022  Show citation