Cystic Fibrosis

Cystic Fibrosis (CF) is a genetic disorder that affects over 70,000 people globally, and is the most common life-shortening genetic disorder in the US. It is caused by a mutation in the cystic fibrosis transmembrane regulator (CFTR) gene and results in the body producing an abnormally thick, sticky mucus which clogs the lungs, making breathing difficult. This can lead to persistent lung infections and damage to the lungs that may require a transplant in some cases. CF affects many other parts of the body too, such as the pancreas, liver, intestines and reproductive organs. There is currently no cure for CF, but treatments such as regular chest physiotherapy and medications, including antibiotics, can help to reduce symptoms and improve quality of life. Research into developing treatments and potentially finding a cure is ongoing and has made great strides in recent years.

← International Journal of Allergy

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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