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Prof. Eitan Kerem and Prof. Michael Wilschanski,

Cystic Fibrosis Center and the Department of Pediatrics,

Hadassah University Medical Center, Mount Scopus Jerusalem


Until now, no drug has been found to correct the defect in the gene or the protein that causes the disease. The current treatment is supportive, aimed at slowing the decline in the lung function by draining the mucous and preventing and treating respiratory infection and inflammation. In addition, supportive treatment includes preservation of a good nutritional condition.




 
          


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