cytomegalovirus

How is CMV Diagnosed in Newborns?

Diagnosis of congenital CMV is typically made through laboratory tests. These include:
PCR (Polymerase Chain Reaction) tests of urine, saliva, or blood to detect CMV DNA
Viral culture
Serological tests to identify CMV-specific antibodies
Early diagnosis is crucial for managing and mitigating the potential long-term effects of the infection.

Frequently asked queries:

What is Cytomegalovirus?
How is CMV Transmitted?
What are the Symptoms of Congenital CMV?
How is CMV Diagnosed in Newborns?
What are the Treatment Options for CMV?
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What are the Long-Term Outcomes for Infants with CMV?
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Why is Fairness Important in Pediatrics?
What Role Does Telemedicine Play in Remote Supervision?
What is a Nuchal Translucency Scan?
What Are the Challenges in Measuring Prevalence?
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What Types of Conditions Are Considered Resource Intensive?
Why are Intranasal Corticosteroids Used in Pediatrics?
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