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Diagnostico de fibrosis quistica en adultos
Diagnostico de fibrosis quistica en adultos

Cystic Fibrosis CF is an autosomal recessive hereditary disease. Early detection combined with early intervention measures have changed the course of this disease with improvements in their survival which has led to a growing population of diagnostico de fibrosis quistica en adultos 18 years. The genetic mutation determines an alteration in Transmembrane Conductance Regulator protein CFTR that affects many organ systems, but the pulmonary involvement is causing increased morbidity and mortality. The most common pathogen that infects adults is Pseudomonas aeruginosa and while there are a number of measures for the management of chronic Pseudomonas infection of therapy aimed at restoring the function of the CFTR protein has gained importance. When respiratory failure progresses only alternative available is lung transplantation improves survival and quality of life in these patients. Edad promedio de sobrevida,
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Diagnostico de fibrosis quistica en adultos
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Diagnostico de fibrosis quistica en adultos
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