Ocular motor signs in an infant with carbohydrate-deficient glycoprotein syndrome type Ia

Am J Ophthalmol. 2000 Oct;130(4):533-5. doi: 10.1016/s0002-9394(00)00569-9.

Abstract

Purpose: To document the evolution of ocular motor abnormalities in an infant with carbohydrate-deficient glycoprotein syndrome.

Methods: Case report. An infant with carbohydrate-deficient glycoprotein syndrome type 1a underwent magnetic resonance imaging and infrared eye movement recording.

Results: A 10-month-old male with carbohydrate-deficient glycoprotein syndrome type Ia had rapid horizontal oscillations of the eyes when startled or awakened from sleep. Clinical examination confirmed this finding and disclosed congenital ocular motor apraxia with a reduced vestibulo-ocular reflex. Infrared eye movement recording showed ocular flutter and square wave jerks superimposed on a horizontal pendular nystagmus. Magnetic resonance imaging showed diffuse cerebellar hypoplasia.

Conclusion: Carbohydrate-deficient glycoprotein syndrome type Ia can be associated with multiple cerebellar eye signs including ocular flutter, square-wave jerks, and congenital ocular motor apraxia.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apraxias / diagnosis
  • Apraxias / etiology*
  • Cerebellum / abnormalities*
  • Congenital Disorders of Glycosylation / complications*
  • Congenital Disorders of Glycosylation / enzymology
  • Eye Movements
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Nystagmus, Pathologic / etiology
  • Ocular Motility Disorders / diagnosis
  • Ocular Motility Disorders / etiology*
  • Phosphotransferases (Phosphomutases) / deficiency
  • Reflex, Vestibulo-Ocular

Substances

  • Phosphotransferases (Phosphomutases)
  • phosphomannomutase