📋Overview
The condition is caused by mutations in the CFTR gene that disrupt the normal movement of salt and water in and out of cells. This genetic defect causes secretions such as mucus, sweat, and digestive enzymes to become thick and sticky instead of acting as thin lubricants.
These dense secretions can obstruct tubes, ducts, and passageways throughout the body, most notably within the respiratory and gastrointestinal systems. The condition is recognized as a chronic, multisystem disease with manifestations that can vary among individuals.
🛡️ Educational information only
This content is provided for general health education and awareness and is based on publicly available medical information. It is not intended to replace professional medical advice, diagnosis, or treatment, and should not be used to make healthcare decisions. Always seek the guidance of a qualified healthcare professional regarding any medical condition, medication, supplement, or procedure.
Additional Resources
Medical codes (for reference)
UMLS CUI: C0010674Codes are provided for reference and interoperability. They are not a diagnosis.
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