Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a type of chronic scarring lung disease characterized by a progressive and irreversible decline in lung function. Symptoms typically include gradual onset of shortness of breath and a dry cough. Other changes may include feeling tired and abnormally large and dome shaped finger and toenails Complications may include pulmonary hypertension heart failure, pneumonia, or pulmonary embolism. The cause is unknown. Risk factors include cigarette smoking, certain viral infections, and a family history of the condition. The underlying mechanism involves scarring of the lungs. Diagnosis requires ruling out other potential causes. It may be supported by a CT scan or lung biopsy which show usual interstitial pneumonia. It is a type of interstitial lung disease.
- Signs and symptoms for Idiopathic pulmonary fibrosis
- Causes for Idiopathic pulmonary fibrosis
- Pathogenesis of Idiopathic pulmonary fibrosis
- Diagnosis for Idiopathic pulmonary fibrosis
- Treatment for Idiopathic pulmonary fibrosis
Related Conference of Idiopathic pulmonary fibrosis
15th International Conference on Pulmonary & Respiratory Medicine
4th International Conference on Tuberculosis, Lung Health and Respiratory Diseases
Idiopathic pulmonary fibrosis Conference Speakers
Recommended Sessions
- Asthma and Allergy
- Chronic Obstructive Pulmonary Disease
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- Emphysema
- Idiopathic pulmonary fibrosis
- Influenza
- Interstistial Lung Disease
- Lung Homeostasis
- Lung transplantation
- Paediatric Pulmonology & Critical care
- Pediatric and Geriatric Gastroenterology
- Pneumonia
- Pulmonary diseases: Treatment, Diagnosis and therapy
- Pulmonary hypertension
- Pulmonary Physiology
- Pulmonary rehabilitation
- Respiratory framework
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