2014
DOI: 10.1002/pd.4362
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Congenital cytomegalovirus infection and small for gestational age infants

Abstract: Congenital CMV infection does not seem to be associated with a higher incidence of SGA, and long-term outcomes do not seem to be affected by isolated impaired fetal growth.

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Cited by 7 publications
(2 citation statements)
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References 32 publications
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“…In addition, a negative IgM result does not necessarily rule out a primary infection with CMV as samples collected too early in the course of a primary infection may not have detectable levels of IgM and it may reappear during reactivation of CMV [27]. On the other hand, the low prevalence of CMV specific IgM is possibly due to the fact that the majority of the women would have recovered from the primary in¬fection, with the loss of IgM, by the time they reach child bearing age 30 Primary CMV infection was identified as sero-conversion in previously CMV seronegative women or by detection of CMVspecific IgM combined with low avidity anti-CMV IgG [31]. Moreover, the pre conception immunity against CMV provides only partial protection from intrauterine transmission of the virus [18].…”
Section: Discussionmentioning
confidence: 99%
“…In addition, a negative IgM result does not necessarily rule out a primary infection with CMV as samples collected too early in the course of a primary infection may not have detectable levels of IgM and it may reappear during reactivation of CMV [27]. On the other hand, the low prevalence of CMV specific IgM is possibly due to the fact that the majority of the women would have recovered from the primary in¬fection, with the loss of IgM, by the time they reach child bearing age 30 Primary CMV infection was identified as sero-conversion in previously CMV seronegative women or by detection of CMVspecific IgM combined with low avidity anti-CMV IgG [31]. Moreover, the pre conception immunity against CMV provides only partial protection from intrauterine transmission of the virus [18].…”
Section: Discussionmentioning
confidence: 99%
“…No other studies of ZIKV-exposed infants have focused on SGA as a risk factor for adverse infant outcomes. In other congenital infections, little has been published about SGA as a risk factor for adverse outcomes [27][28][29]. Approximately 43% of SGA infants were found to have a neurologic, ophthalmologic, or hearing abnormality in comparison to only 18% of NSNM infants (OR, 3.4; 95% CI, 1.1-10.7); 21% had seizures and 43% had abnormal neuroimaging compared to only 16% of NSNM infants (OR, 3.9; 95% CI, 1.2-12.8).…”
Section: Discussionmentioning
confidence: 99%