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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?
How Can CMV be Prevented?
What are the Long-Term Outcomes for Infants with CMV?
What are the Normal Ranges for Biochemical Parameters in Children?
What are the Benefits and Risks?
What is Epiphysiodesis?
What are the Common Types of Fungal Infections in Newborns?
What Factors Influence Inspiratory Time in Pediatrics?
When Should Children be Vaccinated?
How Can Schools Support a Healthy Lifestyle?
When are These Methods Used?
How can MVAs be prevented?
How Can Healthcare Providers Collaborate with NAMI?
How Can Pediatricians Stay Updated on Best Practices?
What Causes Autoimmune Diseases in Children?
Why Are Salads Important for Children?
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