4.6 Article

Initial Description of the Presumed Congenital Zika Syndrome

期刊

AMERICAN JOURNAL OF PUBLIC HEALTH
卷 106, 期 4, 页码 598-600

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AMER PUBLIC HEALTH ASSOC INC
DOI: 10.2105/AJPH.2016.303115

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资金

  1. Brazilian Ministry of Health, Pernambuco State Health Department (SES-PE)
  2. Pan American Health Organization
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq [306489/2010-4, 308311/2009-4, 308590/2013-9]
  4. MRC [MC_PC_15088] Funding Source: UKRI
  5. Medical Research Council [MC_PC_15088] Funding Source: researchfish

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Objectives. To provide an initial description of the congenital syndrome presumably associated with infection by Zika virus compared with other syndromes including congenital infections of established etiologies. Methods. We provide an overview of a published case series of 35 cases, a clinical series of 104 cases, and published and unpublished reports of clinical and laboratory findings describing cases diagnosed since the beginning of the epidemic of microcephaly in Brazil. Results. About 60% to 70% of mothers report rash during pregnancy; mainly in the first trimester. Principal features are microcephaly, facial disproportionality, cutis girata, hypertonia/spasticity, hyperreflexia, and irritability; abnormal neuroimages include calcifications, ventriculomegaly, and lissencephaly. Hearing and visual abnormalities may be present. Conclusions. Preliminary data suggest that severe congenital abnormalities are linked to Zika virus infection. Cases have severe abnormalities, and although sharing many characteristics with congenital abnormalities associated with other viral infections, abnormalities presumably linked to the Zika virus may have distinguishing characteristics. These severe neurologic abnormalities may result in marked mental retardation and motor disabilities for many surviving offspring. Policy Implications. Affected nations need to prepare to provide complex and costly multidisciplinary care that children diagnosed with this new congenital syndrome will require.

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