4 research outputs found
Sequences of oligonucleotide primers used for CMV PCR and sequencing (12,27).
<p>Sequences of oligonucleotide primers used for CMV PCR and sequencing (12,27).</p
UL55 and UL144 genotype distribution of postnatal and congenital CMV infection.
<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.
<p>a. Symptoms of postnatal CMV infection included pneumonia (nβ=β3), and sepsis-like illness with thrombocytopenia (nβ=β2).</p><p>Symptoms of congenital CMV infection included intra-uterine growth retardation (nβ=β5), microcephaly (nβ=β2), hepatosplenomegaly (nβ=β4), petechiae (nβ=β3), jaundice (nβ=β1), seizures (nβ=β1), thrombocytopenia (nβ=β6), anaemia (nβ=β2), and neutropenia (nβ=β1).</p><p>b. MRI was performed in 30 postnatally infected infants and 7 congenitally infected infants. Severe MRI abnormalities included polymicrogyria (nβ=β1), occipital cysts (nβ=β1), ventricular dilatation (nβ=β1) and abnormal white matter signal intensity (nβ=β4).</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.
<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 5β95% coincidence interval. Dots represent outliers.</p