Neuropediatrics 1995; 26(6): 298-305
DOI: 10.1055/s-2007-979778
Original articles

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Neuroradiological and Eye Movement Correlates in Children with Intermittent Saccade Failure: "Ocular Motor Apraxia"

Fatima S. Shawkat1 , D. Kingsley2 , B. Kendall2 , Isabelle Russell-Eggitt1 , D. S. I. Taylor1 , Chr. M. Harris1
  • 1Departments of Ophthalmology, Great Ormond Street Hospital for Children, London WCl 3JH, UK
  • 2Departments of Neuroradiology, Great Ormond Street Hospital for Children, London WCl 3JH, UK
Further Information

Publication History

Publication Date:
19 April 2007 (online)

Abstract

Ocular motor apraxia (OMA) is a clinical sign involving the intermittent inability to initiate saccades, and a failure of quick phases during optokinetic nystagmus (OKN) and vestibular nystagmus (VN). Some patients have no other associated abnormalities (idiopathic), whereas others have a variety of neurological conditions. We quantified the severity of the saccade failure and correlated it with nemo-radiological and other oculomotor findings in 62 children (aged 17 days - 14 years). Saccades, smooth pursuit, OKN and VN were recorded using electrooculography and the extent of "locking up" (absent quick phases during OKN and VN) was measured. Saccades were usually hypo-metric. Pursuit and OKN gains were normal in the majority of the idiopathic cases but were low in those with other neurological conditions. Twenty-four patients had essentially normal scans, whereas 38 had abnormal scans: Delayed myelination, cerebellar abnormalities (particularly involving the vermis), and agenesis of the corpus callosum were the most common findings. A significant positive correlation was present between increasing neuro-radiological deficits and severity of "locking up" during OKN. Principal component analysis showed that brainstem and cerebellar vermis abnormalities were the main factors involved. A pathophysiological basis of OMA is discussed in the light of animal and clinical studies.

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