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Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis [PDF]
Lancet, The, 2008 For more than 20 years, the abnormally thick mucus (mucoviscidosis) in cystic fibrosis has been widely shown to be linked to a genetic defect in the cystic fibrosis transmembrane conductance regulator Cl(-) channel.
Paul M Quinton
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Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege, 1991
Cystic fibrosis is the most frequent autosomic recessive disease in Caucasian population (1/2500). It is characterized by the presence of mucosal plugs in the excretory ducts of the exocrine glands. Pancreatic deficiency with intestinal malabsorption and pulmonary injuries are the main signs of the disease.
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Cystic fibrosis is the most frequent autosomic recessive disease in Caucasian population (1/2500). It is characterized by the presence of mucosal plugs in the excretory ducts of the exocrine glands. Pancreatic deficiency with intestinal malabsorption and pulmonary injuries are the main signs of the disease.
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A case of mucoviscidosis in an adult
British Journal of Diseases of the Chest, 1965Summary Cystic fibrosis rarely presents in adolescence without symptoms in childhood. Such a case is described, and the changing pattern of the disease between childhood and adult life is shown.
E G, ANDERSON, G, LASZLO, H M, BROWN
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