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neurofibromatosis type 1 (nf1)
How Common is NF1 in Neonates?
NF1 is one of the most common genetic disorders, with an incidence of approximately 1 in 3,000 to 1 in 4,000 live births. Although the
clinical manifestations
of NF1 can vary widely, certain signs can be identified in neonates and infants.
Frequently asked queries:
What is Neurofibromatosis Type 1 (NF1)?
How Common is NF1 in Neonates?
What are the Early Signs and Symptoms in Neonates?
How is NF1 Diagnosed in Neonates?
What Research is Currently Being Conducted?
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How are These Services Accessed?
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How Effective Are They in Pediatric Patients?
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