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Application of an Amplitude-integrated EEG Monitor (Cerebral Function Monitor) to Neonates
Published on: September 6, 2017
Value of electrodiagnostic assessment in nonsyndromic microcephaly
L O Atchaneeyasakul1, A Trinavarat, N Wanumkarng
1Department of Ophthalmology, Siriraj Hospital Mahidol University, Bangkok, Thailand. silac@mahidol.ac.th
Insights
Electroretinogram (ERG) and visual evoked potentials (VEP) can reveal visual pathway issues in children with nonsyndromic microcephaly. Abnormal ERG findings are common, but don't always predict poor vision.
Area of Science:
- Ophthalmology
- Neurology
- Pediatrics
Background:
- Nonsyndromic microcephaly is a condition characterized by an abnormally small head size without other associated syndromes.
- Visual impairments are frequently observed in children with microcephaly, but the underlying causes are not always clear.
Purpose of the Study:
- To assess the diagnostic value of electroretinogram (ERG) and visual evoked potentials (VEP) in evaluating visual function in children with nonsyndromic microcephaly.
- To correlate ERG and VEP findings with visual acuity and neuroimaging results.
Main Methods:
- An observational case series involving six children with nonsyndromic microcephaly (aged 8.5 to 158 months).
- Evaluations included flash ERG (photopic, flickering, scotopic, dark-adapted), VEP (flash/pattern-reversal), visual acuity, and ophthalmic examinations.
- Brain CT scans were performed for some participants.
Main Results:
- Three children had normal ERG and VEP responses; two had poor vision, and one showed schizencephaly on CT.
- The other three children exhibited abnormal ERG, primarily with reduced photopic amplitudes.
- Two of these had retinal pigmentary changes, poor vision, brain atrophy, and reduced VEP amplitudes.
Conclusions:
- Abnormal ERG is a frequent finding in nonsyndromic microcephaly, often affecting cone photoreceptors more than rods.
- Reduced ERG amplitudes do not consistently correlate with poor visual acuity.
- Visual dysfunction in these children is likely attributable to posterior visual pathway defects or brain developmental abnormalities.
Purpose:
To evaluate the value of electroretinogram (ERG) and visual evoked potentials (VEP) in children with nonsyndromic microcephaly.
Methods:
In this observational case series, six children with nonsyndromic microcephaly aged 8.5 to 158 months were examined. Main outcome measures included the amplitude of the flash ERG (photopic, flickering, scotopic, and dark-adapted responses), the amplitude and latency of the VEP (flash or pattern-reversal stimulus), visual acuity, slit-lamp biomicroscopy, and indirect ophthalmoscopy.
Results:
Three children demonstrated normal fundus appearances, ERG, and VEP responses: two in this group demonstrated poor vision and brain computed tomography in the third showed schizencephaly. The remaining three children demonstrated abnormal ERG with predominant reduction in photopic amplitudes. Retinal pigmentary granularities were detected in two children in this group, one of whom has poor vision, generalized brain atrophy, and 40% reduction in VEP amplitudes.
Conclusions:
Abnormal ERG is not uncommon among children with nonsyndromic microcephaly. Although cone photoreceptors are affected more than rods, this does not anticipate poor vision. It appears that defects in posterior visual pathway or developmental malformations of the brain should be responsible for poor visual function in nonsyndromic microcephaly.
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