Microcephaly Linked to Significant Developmental Deficits

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Those with postnatal etiology showed worse developmental deficits across all domains.
Those with postnatal etiology showed worse developmental deficits across all domains.

VANCOUVER – Infants with microcephaly face a significant risk of developmental delays and long-term disability, including intellectual disability and cerebral palsy, according to data from a retrospective review presented at the 2016 Child Neurology Society Annual Meeting, October 26-29, 2016 in Vancouver, British Columbia.

With microcephaly top of mind with the emergence of Zika virus, researchers led by Eliza Gordon-Lipkin, MD, of the Kennedy Krieger Institute and Johns Hopkins University School of Medicine in Baltimore, Maryland, sought to better understand the etiologies of microcephaly and its impact on developmental outcomes.

The study included data from 22 infants diagnosed with microcephaly (59.1% female; mean gestational age= 33.79 weeks) from 2006 to 2016. Data from prenatal, perinatal, and neonatal courses as well as NICU follow-up assessments were included in the analysis to yield developmental quotients (DQ). DQs were age-adjusted up to 2 years, with delay defined at DQ<70.

Among the cohort, 55% of infants were preterm, and 41% were characterized as intrauterine growth restricted/ small for gestational age. Approximately 33% had microcephaly at birth (based on data from 12 infants with documented head circumference at birth). Twenty-three percent of etiologies were unknown, while 23% were related to hypoxic-ischemic encephalopathy (HIE); 14% were intracranial hemorrhage (ICH); 14% were structural anomalies; 9% were syndromes; and 5% were related to cytomegalovirus (CMV), herpes simplex virus (HSV) plus hemorrhage, hydrocephalus without hemorrhage, and infart each, respectively.

At follow-up (mean 26.8 months), 73% of infants had delays in one or more areas of development, including gross motor (65%; mean DQ 58.4), fine motor (59%; mean DQ 63.2), and language (59%; mean DQ 65.4), while 45% of infants had delays across all domains. Notably, those with postnatal onset had worse mean DQs across all domains compared to infants with congenital or unknown onsets.

:We don't know how the pathophysiology of each etiology affects outcomes, but that is definitely a future direction to look into,” Dr Gordon-Lipkin told Neurology Advisor, noting that advances in neuroimaging and genetic testing may help to identify unknown etiologies in future studies.

"Interest in this diagnosis is reemerging, and understanding the spectrum of what these infants may present with and what their outcomes may be will provide a foundation for comparison to children with Zika," she said. 

For more coverage of CNS 2016, go here.

Reference

Gordon-Lipkin E, Gentner M, Leppert M. Neurodevelopmental Outcomes in Infants with Microcephaly. Presented at: 2016 Child Neurology Society Annual Meeting. October 26-29, 2016; Vancouver, BC. Abstract 188. 

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