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Updated: Feb 14, 2026

Zika Virus Specific Diagnostic Epitope Discovery
Published on: December 12, 2017
Congenital microcephaly: A diagnostic challenge during Zika epidemics
Jorge L Alvarado-Socarras1, Álvaro J Idrovo2, Gustavo A Contreras-García3
1Neonatal Unit, Department of Pediatrics, Fundación Cardiovascular de Colombia, Floridablanca, Santander, Colombia; Organización Latinoamericana para el Fomento de la Investigación en Salud (OLFIS), Bucaramanga, Santander, Colombia; Colombian Collaborative Network on Zika (RECOLZIKA), Pereira, Risaralda, Colombia.
Abstract:
The multiple, wide and diverse etiologies of congenital microcephaly are complex and multifactorial. Recent advances in genetic testing have improved understanding of novel genetic causes of congenital microcephaly. The recent Zika virus (ZIKV) epidemic in Latin America has highlighted the need for a better understanding of the underlying pathological mechanisms of microcephaly including both infectious and non-infectious causes. The diagnostic approach to microcephaly needs to include potential infectious and genetic etiologies, as well as environmental in-utero exposures such as alcohol, toxins, and medications. Emerging genetic alterations linked to microcephaly include abnormal mitotic microtubule spindle structure and abnormal function of centrosomes. We discuss the diagnostic challenge of congenital microcephaly in the context of understanding the links with ZIKV emergence as a new etiological factor involved in this birth defect.
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