Microcephaly and Zika virus: Neuroradiological aspects, clinical findings and a proposed framework for early evaluation of child development

•Little is known about functioning in infants with microcephaly caused by Zika virus.•An ICF-based framework to assess infants with microcephaly can help early developmental assessment.•Comprehensive assessment is recommended for early identification and intervention. As the recent outbreak of micro...

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Published inInfant behavior & development Vol. 49; pp. 70 - 82
Main Authors Cicuto Ferreira Rocha, Nelci Adriana, de Campos, Ana Carolina, Cicuto Ferreira Rocha, Fellipe, Pereira dos Santos Silva, Fernanda
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2017
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Abstract •Little is known about functioning in infants with microcephaly caused by Zika virus.•An ICF-based framework to assess infants with microcephaly can help early developmental assessment.•Comprehensive assessment is recommended for early identification and intervention. As the recent outbreak of microcephaly cases caused by Zika virus has been declared a global health emergency, providing assessment guidelines for multidisciplinary teams providing early developmental screening and stimulation to infants with microcephaly is much needed. Thus, the aim of this manuscript is to provide an overview on what is known about neuroradiological aspects and clinical findings in infants with microcephaly caused by Zika virus and to propose a framework for early evaluation of child development. The keywords “Zika virus” and “microcephaly” were searched in PubMed database for articles published from incept to May 2017. These texts were reviewed, and the ones addressing neuroradiological and clinical findings in infants were selected. Recommendations for early assessment were made based on the International Classification of Functionality Disability and Health (ICF) model. The database search yielded 599 publications and 36 were selected. The studies detected microcephaly with diffuse brain malformations and calcifications, ventriculomegaly, optic nerve hypoplasia, macular atrophy, cataracts, impaired visual and hearing function, arthrogryposis, spasticity, hyperreflexia, irritability, tremors, and seizures, but very little is known about early development. Early assessments were described based on the ICF domains (Body Function and Structures, Activities and Participation and Contextual factors). Studies published showed abnormal brain, optic, neurologic and orthopedic findings, but very little is known about other aspects of functioning in infants with microcephaly caused by Zika virus. The biopsychosocial model based on the ICF paradigm provides an adequate framework to describe the condition of the infant with microcephaly receiving rehabilitative efforts to minimize disability. Efforts towards early identification of developmental delays should be taken within the first six months of life.
AbstractList As the recent outbreak of microcephaly cases caused by Zika virus has been declared a global health emergency, providing assessment guidelines for multidisciplinary teams providing early developmental screening and stimulation to infants with microcephaly is much needed. Thus, the aim of this manuscript is to provide an overview on what is known about neuroradiological aspects and clinical findings in infants with microcephaly caused by Zika virus and to propose a framework for early evaluation of child development. The keywords "Zika virus" and "microcephaly" were searched in PubMed database for articles published from incept to May 2017. These texts were reviewed, and the ones addressing neuroradiological and clinical findings in infants were selected. Recommendations for early assessment were made based on the International Classification of Functionality Disability and Health (ICF) model. The database search yielded 599 publications and 36 were selected. The studies detected microcephaly with diffuse brain malformations and calcifications, ventriculomegaly, optic nerve hypoplasia, macular atrophy, cataracts, impaired visual and hearing function, arthrogryposis, spasticity, hyperreflexia, irritability, tremors, and seizures, but very little is known about early development. Early assessments were described based on the ICF domains (Body Function and Structures, Activities and Participation and Contextual factors). Studies published showed abnormal brain, optic, neurologic and orthopedic findings, but very little is known about other aspects of functioning in infants with microcephaly caused by Zika virus. The biopsychosocial model based on the ICF paradigm provides an adequate framework to describe the condition of the infant with microcephaly receiving rehabilitative efforts to minimize disability. Efforts towards early identification of developmental delays should be taken within the first six months of life.
•Little is known about functioning in infants with microcephaly caused by Zika virus.•An ICF-based framework to assess infants with microcephaly can help early developmental assessment.•Comprehensive assessment is recommended for early identification and intervention. As the recent outbreak of microcephaly cases caused by Zika virus has been declared a global health emergency, providing assessment guidelines for multidisciplinary teams providing early developmental screening and stimulation to infants with microcephaly is much needed. Thus, the aim of this manuscript is to provide an overview on what is known about neuroradiological aspects and clinical findings in infants with microcephaly caused by Zika virus and to propose a framework for early evaluation of child development. The keywords “Zika virus” and “microcephaly” were searched in PubMed database for articles published from incept to May 2017. These texts were reviewed, and the ones addressing neuroradiological and clinical findings in infants were selected. Recommendations for early assessment were made based on the International Classification of Functionality Disability and Health (ICF) model. The database search yielded 599 publications and 36 were selected. The studies detected microcephaly with diffuse brain malformations and calcifications, ventriculomegaly, optic nerve hypoplasia, macular atrophy, cataracts, impaired visual and hearing function, arthrogryposis, spasticity, hyperreflexia, irritability, tremors, and seizures, but very little is known about early development. Early assessments were described based on the ICF domains (Body Function and Structures, Activities and Participation and Contextual factors). Studies published showed abnormal brain, optic, neurologic and orthopedic findings, but very little is known about other aspects of functioning in infants with microcephaly caused by Zika virus. The biopsychosocial model based on the ICF paradigm provides an adequate framework to describe the condition of the infant with microcephaly receiving rehabilitative efforts to minimize disability. Efforts towards early identification of developmental delays should be taken within the first six months of life.
Author de Campos, Ana Carolina
Cicuto Ferreira Rocha, Fellipe
Cicuto Ferreira Rocha, Nelci Adriana
Pereira dos Santos Silva, Fernanda
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Keywords International Classification of Functionality Disability and Health
Infant
Zika virus
Microcephaly
Early development
Language English
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Snippet •Little is known about functioning in infants with microcephaly caused by Zika virus.•An ICF-based framework to assess infants with microcephaly can help early...
As the recent outbreak of microcephaly cases caused by Zika virus has been declared a global health emergency, providing assessment guidelines for...
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SubjectTerms Brain - virology
Child
Child Development - physiology
Early development
Female
Humans
Infant
International Classification of Functionality Disability and Health
Microcephaly
Microcephaly - virology
Zika virus
Zika Virus - pathogenicity
Zika Virus Infection - diagnostic imaging
Title Microcephaly and Zika virus: Neuroradiological aspects, clinical findings and a proposed framework for early evaluation of child development
URI https://dx.doi.org/10.1016/j.infbeh.2017.07.002
https://www.ncbi.nlm.nih.gov/pubmed/28755567
Volume 49
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