TABLE 3.
Congenital anomalies potentially related to maternal ZIKV infection.
Brain Abnormalities • Congenital microcephaly: HC < 3rd centile for gestational age and sex • Intracranial calcifications • Cerebral atrophy • Abnormal cortical formation (lissencephaly, polymicrogyria, pachygyria, schizencephaly, and gray matter heterotopia) • Corpus callosum abnormalities • Cerebellar abnormalities • Porencephaly • Hydranencephaly • Ventriculomegaly* or hydrocephaly* • Fetal brain disruption sequence (severe microcephaly, collapsed skull, overlapping sutures, scalp redundancy) • Other major brain abnormalities (thalamus, hypothalamus, pituitary, basal ganglia, or brainstem) |
Neural Tube Defects and Other Early Brain Malformations** • Anencephaly or acrania • Encephalocele • Spina bifida without anencephaly • Holoprosencephaly or arhinencephaly |
Eye Abnormalities • Microphthalmia or anopthalmia • Coloboma • Congenital cataract • Intraocular calcifications • Chorioretinal anomalies (e.g., atrophy, scarring, macular pallor, retinal hemorrhage and gross pigmentary changes excluding retinopathy of prematurity) • Optic nerve atrophy, pallor and other optic nerve abnormalities |
Consequences of Central Nervous System Dysfunction • Congenital contractures (e.g., arthrogryposis, club foot, congenital hip dysplasia) with associated brain abnormalities • Congenital sensorineural hearing loss documented by postnatal testing |
Table adapted from the US Centers for Disease Control standard case definition for birth defects potentially associated with ZIKV infection (World Health Organization (WHO)., 2018a). *Excludes isolated mild ventriculomegaly without other brain abnormalities or hydrocephalus due to hemorrhage. **Evidence for a link between ZIKV infections and neural tube defects is weaker than for other listed anomalies.