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Cystic Fibrosis is an inherited genetic disease that affects about 1 infant 2500-2700 , therefore, is a genetic disease that can be defined as rare and is transmitted with autosomal recessivoi mechanism . The cause of the disease is a defect in the CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) whose function EDI regular exchanges electrolyte . The alteration of the protein leads to an abnormality of transport of salts and determines mainly the production of secretions " dehydrated " : the sweat is very rich in sodium and chlorine , the mucus is thick and sticky and tends to clog the ducts in which it is to be . To be affected by the effects of the disease are primarily respiratory , airways , pancreas , liver , intestines, and the reproductive system, especially in males due to obstruction of the sperm duct
     
 
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