Cystic Fibrosis

Cystic Fibrosis (CF) is a genetic disorder that affects the way the body produces and transports a type of protein known as mucus. It is a life-threatening condition that affects the lungs, digestive system, and other organs. Symptoms vary from person to person, but can include frequent lung infections, difficulty breathing, and poor digestion. In severe cases, it may lead to respiratory failure, malnutrition, and even death. Treatment is aimed at managing symptoms and improving quality of life, and involves antibiotics, airway clearance techniques, and nutritional supplements. With advances in medical care, many people living with CF have longer life expectancy and a better quality of life.

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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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