4 research outputs found

    UL55 and UL144 genotype distribution of postnatal and congenital CMV infection.

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    <p>a. In two postnatally infected infants only UL144 or UL55 could be genotyped.</p><p>UL55 and UL144 genotype distribution of postnatal and congenital CMV infection.</p

    Demographic and clinical characteristics of 58 postnatally and 13 congenitally infected infants.

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    <p>a. Symptoms of postnatal CMV infection included pneumonia (nβ€Š=β€Š3), and sepsis-like illness with thrombocytopenia (nβ€Š=β€Š2).</p><p>Symptoms of congenital CMV infection included intra-uterine growth retardation (nβ€Š=β€Š5), microcephaly (nβ€Š=β€Š2), hepatosplenomegaly (nβ€Š=β€Š4), petechiae (nβ€Š=β€Š3), jaundice (nβ€Š=β€Š1), seizures (nβ€Š=β€Š1), thrombocytopenia (nβ€Š=β€Š6), anaemia (nβ€Š=β€Š2), and neutropenia (nβ€Š=β€Š1).</p><p>b. MRI was performed in 30 postnatally infected infants and 7 congenitally infected infants. Severe MRI abnormalities included polymicrogyria (nβ€Š=β€Š1), occipital cysts (nβ€Š=β€Š1), ventricular dilatation (nβ€Š=β€Š1) and abnormal white matter signal intensity (nβ€Š=β€Š4).</p><p>Demographic and clinical characteristics of 58 postnatally and 13 congenitally infected infants.</p

    Log<sub>10</sub> CMV urine load in postnatally and congenitally infected infants.

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    <p>Bar in boxplot represent median viral load after log<sub>10</sub> transformation. Upper and lower limit of boxplot represent 75<sup>th</sup> and 25<sup>th</sup> percentile, respectively. Whiskers represent 5–95% coincidence interval. Dots represent outliers.</p
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