4.7 Article

Congenital Zika Syndrome: Genetic Avenues for Diagnosis and Therapy, Possible Management and Long-Term Outcomes

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 11, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/jcm11051351

Keywords

Zika virus; pregnancy; microcephaly; prenatal diagnosis; neuroimaging; long-term outcomes; single nucleotide polymorphisms (SNPs)

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This review focuses on different aspects of congenital Zika virus (ZIKV) infection, with a special emphasis on the long-term clinical and neuroimaging outcomes in children. The study highlights that the pathogenesis of the disease is not fully understood and the clinical signs are not limited to microcephaly. The authors propose optimization of diagnostic protocols in endemic countries and emphasize the importance of early diagnosis and appropriate management of chronic problems. Further research and long-term follow-up are needed to improve treatment strategies for this relatively recently discovered congenital infectious syndrome.
Zika virus (ZIKV) was discovered in Uganda in 1947 and was originally isolated only in Africa and Asia. After a spike of microcephaly cases in Brazil, research has closely focused on different aspects of congenital ZIKV infection. In this review, we evaluated many aspects of the disease in order to build its natural history, with a focus on the long-term clinical and neuro-radiological outcomes in children. The authors have conducted a wide-ranging search spanning the 2012-2021 period from databases PubMed, PubMed Central, Web of Science, Medline, Scopus. Different sections reflect different points of congenital ZIKV infection syndrome: pathogenesis, prenatal diagnosis, clinical signs, neuroimaging and long-term developmental outcomes. It emerged that pathogenesis has not been fully clarified and that the clinical signs are not only limited to microcephaly. Given the current absence of treatments, we proposed schemes to optimize diagnostic protocols in endemic countries. It is essential to know the key aspects of this disease to guarantee early diagnosis, even in less severe cases, and an adequate management of the main chronic problems. Considering the relatively recent discovery of this congenital infectious syndrome, further studies and updated long-term follow-up are needed to further improve management strategies for this disease.

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