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Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Nystagmus secondary to drug exposure in utero
Alan O Mulvihill1, Peter D Cackett, Nick D George
1Princess Alexandra Eye Pavilion, Chalmers Street, Edinburgh EH3 9HA, UK.
Insights
Infant nystagmus can be linked to prenatal exposure to opiates and benzodiazepines. Combined exposure may increase risks, suggesting these drugs should be considered in diagnosing infantile nystagmus.
Area of Science:
- Ophthalmology
- Neonatology
- Teratology
Background:
- Prenatal exposure to substances can impact infant development.
- Infantile nystagmus is a vision disorder characterized by involuntary eye movements.
- Opiate and benzodiazepine misuse during pregnancy is a growing concern.
Purpose of the Study:
- To investigate the occurrence of infantile nystagmus in infants exposed to opiates and/or benzodiazepines in utero.
- To describe associated ocular and systemic findings in these infants.
Main Methods:
- A clinical examination and casenote review was conducted.
- The study included 14 infants diagnosed with nystagmus.
- Mothers of these infants reported opiate and/or benzodiazepine misuse during pregnancy.
Main Results:
- 12 infants were exposed to opiates, 9 also to benzodiazepines; 2 were exposed to benzodiazepines alone.
- Nystagmus was primarily fine horizontal pendular or jerk, with onset in the first 6 months.
- Associated findings included developmental delay (64.3%), delayed visual maturation (50%), microcephaly (42.9%), and optic nerve hypoplasia (14.3%).
Conclusions:
- A teratogenic association exists between in utero exposure to opiates/benzodiazepines and infantile nystagmus.
- Combined opiate and benzodiazepine exposure appears particularly linked to nystagmus and associated features.
- Prenatal exposure to these substances should be considered in the differential diagnosis of infantile nystagmus.
Aim:
To report the occurrence of nystagmus in children exposed to opiates and/or benzodiazepines during pregnancy, and to describe the associated ocular and systemic findings.
Methods:
Clinical examination and casenote review of 14 children with nystagmus whose mothers had misused opiates and/or benzodiazepines during pregnancy.
Results:
Twelve children were exposed to opiates during pregnancy, of whom nine had also been exposed to benzodiazepines. Two children were exposed to benzodiazepines alone. In the primary position, the nystagmus was a fine horizontal pendular type in 10 (71.4%) children and was a fine horizontal jerk nystagmus in the other 4 (28.6%) children. The onset of the nystagmus probably occurred in the first 6 months of life in all cases. The mean binocular best-corrected logarithm of the minimum angle of resolution visual acuity was 0.59 (20/80). Electroretinogram and visual evoked potential examinations were found to be normal in the three children tested. Nine (64.3%) children had developmental delay and at least 7 (50%) had delayed visual maturation. Six children had microcephaly and two had bilateral optic nerve hypoplasia. None of the children had a specific neurological diagnosis or seizure disorder.
Conclusion:
This study strongly supports a teratogenic association between exposure to controlled drugs in utero and infantile nystagmus. Furthermore, the nystagmus and associated clinical features seem to be particularly associated with combined use of opiates and benzodiazepines. Exposure to opiates and/or benzodiazepines during pregnancy should be considered in the differential diagnosis of infantile nystagmus.
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