How is the CFTR Gene Related to Neonatal Disorders?
Mutations in the CFTR gene can cause a condition known as Cystic Fibrosis (CF), a severe genetic disorder that affects the respiratory, digestive, and reproductive systems. In neonates, CF can present with a variety of symptoms, including meconium ileus, which is a blockage of the small intestine by thick, sticky meconium. Early diagnosis and intervention are crucial for managing the symptoms and improving the quality of life.
