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Congenital infection with human herpesvirus 6 variant B associated with neonatal seizures and poor neurological outcome
Author(s) -
Lanari Marcello,
Papa Irene,
Venturi Valentina,
Lazzarotto Tiziana,
Faldella Giacomo,
Gabrielli Liliana,
Guerra Brunella,
Landini Maria Paola,
Salvioli Gian Paolo
Publication year - 2003
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.10441
Subject(s) - medicine , meningoencephalitis , cerebrospinal fluid , hyperintensity , ventriculomegaly , pathology , subclinical infection , encephalitis , virology , magnetic resonance imaging , pediatrics , virus , fetus , pregnancy , biology , radiology , genetics
Human herpesvirus 6 (HHV 6) has neurotropic and neuroinvasive properties. The virus has been found in the cerebrospinal fluid of many children with aseptic meningoencephalitis. Intrauterine transmission has been documented by HHV 6 DNA detection in cord blood specimens of apparently healthy newborns and in fetuses following spontaneous abortions. A patient is described with early neonatal afebrile seizures resulting from a congenital HHV 6 variant B infection disclosed by repeated detection of viral genome by polymerase chain reaction (PCR) in cerebrospinal fluid in the first days of life. At follow‐up, magnetic resonance imaging (MRI) studies disclosed hyperintensities in the periventricular white matter and basal ganglia, associated with cerebral atrophy. Further follow‐up at 18 months revealed poor neurological outcome with mild neurodevelopmental retardation, strabismus and hypertonia of legs. This report provides evidence of neurological involvement after HHV 6 vertical transmission, and the association with neurological sequelae. J. Med. Virol. 70:628–632, 2003. © 2003 Wiley‐Liss, Inc.

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