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3,583 Possible Causes for Cystic Fibrosis, Tracheal Tug

  • Bronchiolitis

    Please email any questions to: Cystic Fibrosis (London Chest Physiotherapy ) Cystic fibrosis also called mucoviscidosis affects the lungs and digestive[] tug Nasal flaring Marked increase or decrease Tracheal tug Nasal flaring Accessory Muscle Use None or minimal Moderate chest wall retraction Marked chest wall retraction[] Premature babies and babies with congenital heart disease or cystic fibrosis are at greater risk of becoming ill with this infection.[]

  • Thoracic Aortic Aneurysm

    Learn more about Pediatric Cardiology Pediatric Cystic Fibrosis Each member of our cystic fibrosis, or CF, team is passionate about providing patients the most comprehensive[] tug), and tracheal deviation.[] Learn more about Pediatric Cystic Fibrosis Pediatric Hematology and Oncology Pediatric Infectious Diseases Pediatric Nephrology Pediatric Neurology Pediatric neurologists[]

  • Bronchitis

    Abstract Aspergillus fumigatus frequently colonizes the airways of patients with cystic fibrosis (CF) and may cause various severe infections, such as bronchitis.[] Cystic fibrosis patients are known to produce abundant, purulent sputum consisting mainly of DNA and cellular debris.[] Electronic address: 2 Cystic Fibrosis Support Centre, Department of Pediatrics, University of Brescia, Brescia, Italy.[]

    Missing: Tracheal Tug
  • Acute Bronchitis

    Acute inflammation of the tracheobronchial tree in patients with underlying chronic bronchial disorders (eg, COPD, bronchiectasis, cystic fibrosis ) is considered an acute[] If people who have chronic lung disorders such as COPD, bronchiectasis, or cystic fibrosis develop inflammation of their trachea and bronchi, the inflammation is considered[] fibrosis If you're prescribed antibiotics for bronchitis, it's likely to be a five-day course of amoxicillin or doxycycline.[]

    Missing: Tracheal Tug
  • Sinusitis

    Emphasis was also placed on identifying multiple chronic conditions that would modify management of rhinosinusitis, including asthma, cystic fibrosis, immunocompromised state[] The Sinuses in Cystic Fibrosis The sinuses are a group of 4 pairs of air filled spaces in the head.[] The complications of cystic fibrosis, gastroesophageal reflux, or HIV and other immune system-related diseases can result in nasal blockage.[]

    Missing: Tracheal Tug
  • Pseudomonas

    Pseudomonas aeruginosa is the key bacterial agent of cystic fibrosis (CF) lung infections, and the most important pathogen in progressive and severe CF lung disease.[] PCN is readily recovered in large quantities in sputum from patients with cystic fibrosis who are infected by P. aeruginosa.[] fibrosis centres and recreation camps. 15-17 P cepacia can cause respiratory tract infection in cystic fibrosis, 8 18 although it is much less common in non-cystic fibrosis[]

    Missing: Tracheal Tug
  • Atelectasis

    INTRODUCTION: Recombinant human deoxyribonuclease (rhDNase) reduces sputum viscosity and improves pulmonary function in cystic fibrosis (CF).[] Mucus plugs are also common in children, people with cystic fibrosis and during severe asthma attacks. Foreign body.[] Recombinant human DNase (rhDNase) is an established treatment of atelectasis in cystic fibrosis and its use is also reported in the management of asthma, respiratory syncitial[]

    Missing: Tracheal Tug
  • Cholelithiasis

    Cystic Fibrosis Abnormal Biliary Anatomy Hepatobiliary Disease Crohn’s Disease Or other condition that affects the terminal ileum Systemic Infection / Sepsis Congenital Heart[] fibrosis, and Native American ethnicity.[] fibrosis because of bile salt malabsorption) or in lecithin secretion (eg, in a rare genetic disorder that causes a form of progressive intrahepatic familial cholestasis)[]

    Missing: Tracheal Tug
  • Osteoporosis

    The average woman loses up to 10 per cent of Read more on Australasian Menopause Society website Bisphosphonates for osteoporosis in people with cystic fibrosis Cochrane Cystic[] fibrosis, osteogenesis imperfecta, homocystinuria, Ehlers-Danlos syndrome, Marfan syndrome, hemochromatosis, hypophosphatasia Other - Porphyria, sarcoid, immobilization,[] Genetic disorders - Marfan syndrome, osteogenesis imperfecta, hypophosphatasia, cystic fibrosis, glycogen storage diseases, hemochromatosis, and homocystinuria are examples[]

    Missing: Tracheal Tug
  • Chronic Obstructive Pulmonary Disease

    […] caused by genetic mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.[] ABPA is a complicating factor in 2% of patients with asthma and is also seen in patients with cystic fibrosis.[] Recent research suggests they play a role in exacerbations of cystic fibrosis (CF).[]

    Missing: Tracheal Tug

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