Literature DB >> 34661750

Two-year follow-up of children with congenital Zika syndrome: the evolution of clinical patterns.

Erica Conti Rua1, Solange Artimos de Oliveira2, Renata Artimos de Oliveira Vianna2, Luis Antonio Bataglin Dalcastel2, Teresa Cristina de Castro Sarmet Dos Santos2, Claudete Aparecida Araújo Cardoso2, Alexandre Ribeiro Fernandes2.   

Abstract

The aim of the study was to describe neurological manifestations in children with congenital Zika syndrome (CZS) in the first 2 years of age. In this prospective observational study, children with CZS treated at a university hospital received a neurological assessment and were evaluated using two neurodevelopmental scales (the Denver II test and the assessment of gross motor development of the World Health Organization) by a pediatric neurologist on admission to the study and at 4, 8, 12, 18, and 24 months of age. The data collected were stored in Microsoft Excel version 14.6.3. Thirty-eight children (27 males and 11 females; a median age of 4.3 months (interquartile range (IQR): 1.6-11.4)) with CZS were evaluated. Irritability was present in 50% and 27% of the children at 8 months and 24 months, respectively. Axial hypertonia was highly prevalent at 4 months (77%), with a decrease to 50% at 24 months. At all ages, spastic tetraparesis was the most common motor abnormality (> 80%). Twenty-seven (71%) participants were diagnosed with epilepsy, and the median age at seizure onset was 6 months (IQR: 3.5-8). The most frequent types of seizures were focal seizures and spasms, with spasms being the most frequent in the first year of life (52%) and focal crises being the most frequent in the second year of life (50%).
Conclusion: This study allowed observation of neurological abnormalities over time, the evolution of epileptic manifestations, and recognition of new patterns of clinical neurological abnormalities, helping clinicians to recognize CZS earlier, minimizing the impact of new outbreaks. What is Known: • Clinical patterns of SZC patients at pre-established ages or date of data collection • More frequent studies with data collection of clinical-radiological features of patient's over his first year of life What is New: • Comprehensive clinical neurological progression data regarding CZS in the first 2 years of life, recognizing patterns • Hypothesis including a new CZS spectrum with milder clinical-radiological features.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Cerebral palsy; Congenital Zika syndrome; Microcephaly

Mesh:

Year:  2021        PMID: 34661750     DOI: 10.1007/s00431-021-04280-z

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  2 in total

1.  Movement disorders in children with congenital Zika virus syndrome.

Authors:  Hélio van der Linden; Laura Silveira-Moriyama; Vanessa van der Linden; André Pessoa; Kette Valente; Jonathan Mink; Alex Paciorkowski
Journal:  Brain Dev       Date:  2020-07-16       Impact factor: 1.961

2.  Zika: A scourge in urban slums.

Authors:  Robert E Snyder; Claire E Boone; Claudete A Araújo Cardoso; Fabio Aguiar-Alves; Felipe P G Neves; Lee W Riley
Journal:  PLoS Negl Trop Dis       Date:  2017-03-23
  2 in total
  1 in total

1.  TGF-β1 Promotes Zika Virus Infection in Immortalized Human First-Trimester Trophoblasts via the Smad Pathway.

Authors:  Quang Duy Trinh; Ngan Thi Kim Pham; Kazuhide Takada; Chika Takano; Shihoko Komine-Aizawa; Satoshi Hayakawa
Journal:  Cells       Date:  2022-09-27       Impact factor: 7.666

  1 in total

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