Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease sandifer syndrome
Phenotype C0013421|dystonia
Sentences 1
PubMedID- 23897137 In this paper we analyze paroxysmal motor phenomena in awake children, dividing them according to their clinical manifestations: extrapyramidal episodes (paroxysmal kinesiogenic, non kinesiogenic and not related to exercise dyskinesias, dopa responsive dystonia) and similar symptoms of dystonia (sandifer syndrome); manifestations of startle (hyperekplexia); episodic eye and head movements (benign paroxysmal tonic upward gaze nistagmus deviation); episodic ataxia (familial episodic ataxias, paroxysmal benign vertigo); stereotyped and phenomena of self-gratification; and myoclonic events (benign myoclonus of early infancy).

Page: 1