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Familial congenital oculomotor apraxia: clinical and electro-oculographic features.

Abstract
The electro-oculographic (EOG) features of both horizontal and vertical eye movements in congenital oculomotor apraxia (COMA) were not previously reported. A girl referred to the ophthalmologic department for abnormal eye movements was diagnosed as COMA. The same abnormal ocular movements were observed in her younger sister and her father who was unaware of his difficulties to initiate voluntary saccades. When performed, EOG recordings of all horizontal and vertical saccadic eye movements were severely altered whatever the age of the patient. Pursuit was normal for these patients. It confirms that the control of saccadic eye movements is still altered in adults in both directions horizontal and vertical that were never reported. EOG is necessary to rule out inherited form of this saccade initiation failure.
AuthorsChristophe Orssaud, Isabelle Ingster-Moati, Olivier Roche, Emmanuel Bui Quoc, Jean Louis Dufier
JournalEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society (Eur J Paediatr Neurol) Vol. 13 Issue 4 Pg. 370-2 (Jul 2009) ISSN: 1532-2130 [Electronic] England
PMID18703363 (Publication Type: Case Reports, Journal Article)
Topics
  • Adult
  • Apraxias (complications, diagnosis, genetics)
  • Child, Preschool
  • Electrooculography (methods)
  • Family Health
  • Female
  • Humans
  • Infant
  • Male
  • Ocular Motility Disorders (complications, diagnosis, genetics)

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