Cystic fibrosis is an inherited genetic disorder caused by mutations in the CFTR gene. It leads to the production of thick, sticky mucus that can clog the lungs and digestive tract, resulting in breathing difficulties, frequent infections, and problems absorbing nutrients.
Symptoms may appear in infancy or later in life. Common signs include:
Cystic fibrosis arises when both parents carry and pass on a defective CFTR gene. Key points are:
At GastroDoxs, our dedicated cystic fibrosis team in Jersey Village delivers personalized, multidisciplinary care designed to help you breathe easier and thrive. From advanced CFTR modulator therapies to tailored nutrition plans and airway clearance techniques, we partner with you and your family every step of the way. Ready to take control of your health? Book an appointment today and let us create a comprehensive CF management plan that fits your lifestyle.
We've successfully treated more than 1k patients, helping individuals improve their digestive health and overall well-being through expert, personalized care.
With over 20 years of experience, GastroDoxs has been a trusted provider of gastroenterology care, focusing on delivering the best outcomes for patients
Dr. Bharat Pothuri is a Board-Certified Gastroenterologist and Hepatologist. With extensive experience in digestive health, he specializes in advanced endoscopic procedures, chronic GI disorder management, and preventive care. Dr. Pothuri is dedicated to providing expert, patient-focused insights to help improve gut health and overall well-being.
The ICD-10 codes for cystic fibrosis fall under E84.0-E84.9. Each subcode specifies the organ systems involved (pulmonary, digestive, with meconium ileus, etc.). Your provider or medical coder will select the exact code based on your symptoms and complications.
No. Cystic fibrosis is an inherited genetic disorder caused by mutations in the CFTR gene. It cannot be spread from person to person.
Diagnosis typically involves newborn screening, a sweat chloride test to measure salt levels in sweat, and genetic testing to identify CFTR mutations. In some cases, additional lung function tests or imaging may be used.
Many infants show signs within the first few weeks of life. Common early indicators include difficulty passing meconium, poor weight gain, greasy stools, and recurrent respiratory infections.
With modern therapies and comprehensive care, many people with cystic fibrosis now live into their 40s, 50s, and beyond. Life expectancy varies based on the severity of lung disease, nutrition, and access to specialized treatments.
Yes. A local CF specialist team provides tailored treatment plans, convenient follow-up appointments, and coordinated care with respiratory therapists, dietitians, and genetic counselors.
Most CF patients are seen every 3 to 4 months for routine evaluations. If you experience frequent lung infections or nutritional issues, your provider may recommend more frequent visits.
Good nutrition is vital-high-calorie, high-protein meals and fat-soluble vitamins help-but dietary management must be combined with medications, airway clearance, and other therapies for optimal health.
Yes. CFTR modulators (such as ivacaftor, lumacaftor, tezacaftor, and elexacaftor) target the underlying protein defect. Ongoing research includes gene therapy and novel anti-inflammatory drugs.
Our billing and insurance specialists can walk you through the relevant codes and help with claims. You can also consult resources like the CMS website or professional coding manuals for detailed ICD-10 guidance.
