A Possible Association Between Zika Virus Infection and CDK5RAP2 Mutation.

CDK5RAP2 Colombia Zika virus brain abnormalities microcephaly vertical transmission whole-exome sequencing

Journal

Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621

Informations de publication

Date de publication:
2021
Historique:
received: 27 01 2020
accepted: 27 01 2021
entrez: 5 4 2021
pubmed: 6 4 2021
medline: 6 4 2021
Statut: epublish

Résumé

Flaviviridae family belongs to the Spondweni serocomplex, which is mainly transmitted by vectors from the We report a case of a 28-year-old Colombian woman, who came to the Obstetric Department with an assumed conglomerate of fetal abnormalities detected We used molecular and microbiological assessments to report the initial case of vertically transmitted ZIKV infection with congenital syndrome associated with a neurological syndrome, where a mutation in the

Identifiants

pubmed: 33815457
doi: 10.3389/fgene.2021.530028
pmc: PMC8018576
doi:

Types de publication

Journal Article

Langues

eng

Pagination

530028

Informations de copyright

Copyright © 2021 Candelo, Sanz, Ramirez-Montaño, Diaz-Ordoñez, Granados, Rosso, Nevado, Lapunzina and Pachajoa.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Estephania Candelo (E)

Universidad Icesi, Ear Institute University College London and Fundación Valle del Lili, Cali, Colombia.
Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Colombia.

Ana Maria Sanz (AM)

Fundacion Valle del Lili, Cali, Colombia.

Diana Ramirez-Montaño (D)

Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Colombia.

Lorena Diaz-Ordoñez (L)

Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Colombia.

Ana Maria Granados (AM)

Neuroradiology Department Fundación Valle del Lili, Cali, Colombia.

Fernando Rosso (F)

Fundacion Valle del Lili, Cali, Colombia.

Julian Nevado (J)

Instituto de Genética Médica y Molecular (INGEMM), IdiPAZ, HospitalUniversitario La Paz, Madrid, CIBER de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain.

Pablo Lapunzina (P)

Instituto de Genética Médica y Molecular (INGEMM), IdiPAZ, HospitalUniversitario La Paz, Madrid, CIBER de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain.

Harry Pachajoa (H)

Center for Research on Congenital Anomalies and Rare Diseases (CIACER), Department of Basic Medical Sciences, Universidad Icesi, Cali, Colombia.
Genetics Department, Fundación Valledel Lili, Cali, Colombia.

Classifications MeSH