Optic nerve hypoplasia, encephalopathy, and neurodevelopmental handicap.
retrospective_cohort · Level III
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- Record sourced from PubMed, PMID 2021594.
- Also identified by PMC identifier 1042331.
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Abstract
Abnormalities of the central nervous system are frequently described in optic nerve hypoplasia. In a longitudinal study of 46 consecutive children (32 term, 14 preterm) with bilateral optic nerve hypoplasia 32 (69.5%) had associated neurodevelopmental handicap. Of these, 90% had structural central nervous system abnormalities on computed tomographic brain scans. Neurodevelopmental handicap occurred in 62.5% of the term and 86% of the preterm infants respectively. Term infants had a greater incidence of ventral developmental midline defects and proportionately fewer maternal and/or neonatal complications throughout pregnancy, while encephaloclastic lesions were commoner among the premature infants. An association of optic nerve hypoplasia with the twin transfusion syndrome and prenatal vascular encephalopathies is described.
Medical subject headings
- Abnormalities, Multiple
- Brain
- Cerebral Palsy
- Epilepsy
- Intellectual Disability
- Optic Nerve