Cystic Fibrosis

Cystic fibrosis (CF) is a hereditary disorder that affects the lungs, digestive system and other organs in the body. It is caused by a faulty gene, meaning that it is passed down from parents to children. CF is characterized by abnormally thick and sticky mucus that clogs and damages organs. Common symptoms of CF include breathlessness, salty-tasting skin, frequent lung infections and poor weight gain. Treatment for CF includes medications, airway clearance techniques, physical therapy and possibly lung transplant. With advances in medical science, life expectancy for people living with CF has drastically improved.

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Related Articles

12 article(s) found
Coexistence of Mature Cystic Teratoma and Endometrioma in an Ovarian Cyst
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Non-Syndromic Multiple Keratocystic Odontogenic Tumor: A Case Report
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Management of Arthrofibrosis of the Knee after an Arthroscopic Meniscectomy with Paralytic Shellfish Poisoning Toxin. Case Report.
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Action Mechanisms and Therapeutic Targets of Renal Fibrosis
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Hirsutism and Anthropometric Profiles Among Subjects with Polycystic Ovarian Morphology? A Cross-Sectional Analysis
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A Rare Cause of Acute Renal Failure: Retroperitoneal Fibrosis
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Glandular and Cystic Bladder Cystitis: Case Report and Review of the Literature
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Fetal Abdominal Cystic Lesion: A Diagnostic Dilemma and Prognostic Challenge-Report of Two Cases of Mesentric Lymphangioma with Review of Literature
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Hepatic Cysts as a Manifestation of Polycystic Kidney Disease (Polycystic Liver Report of 2 Mother-Son Cases)
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Evaluation of Cinnamon Supplementation on Insulin Resistance, BMI and Estradiol Levels in Women with Polycystic Ovary Syndrome: A Double-Blinded Randomized Controlled Clinical Trial
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Evolution of Janus Kinase 2 V617F-negative idiopathic myelofibrosis into Philadelphia+ chronic myeloid leukemia
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Adenoid Cystic Carcinoma of the Lacrimal Gland in a 36 year Old Male
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