A positive CF screen means that your baby has two gene changes that cause Cystic Fibrosis.
Based on information from medical screening processes, a result indicating that a screen is CF positive means a specific genetic finding has been made.
According to screening guidelines:
- A positive screen indicates that your baby has two gene changes that cause CF.
This result doesn't immediately diagnose the severity of the condition but signifies the genetic basis for it.
What Happens After a Positive CF Screen?
Receiving a positive CF screen result is the first step in understanding a baby's potential health picture regarding Cystic Fibrosis. It requires further medical attention and testing to confirm the diagnosis and determine the specific implications.
Key follow-up steps typically include:
- Consultation with a Specialist: Your baby will need to see a doctor who specializes in Cystic Fibrosis to get expert evaluation and guidance.
- Additional Testing: Results from the initial newborn screening may necessitate further tests. One crucial test commonly performed is the sweat test, which measures the amount of salt in sweat – a key indicator in diagnosing CF.
- Determining Impact: The specialist doctor will work to determine how the condition might affect your baby based on the specific gene changes found and the results of follow-up tests.
Understanding a positive CF screen result is vital for accessing timely and appropriate medical care for your baby.
