SUMMARYNine patients with Cystic Fibrosis attended at Hospital Nacional Cayetano Heredia, Lima-Perú, from January 1990 to May 1994, are presented. At the time of the diagnosis they were between 10 months to 12 years; 6 were females; 5 were hospitalized; 3 were caucasic, 2 were diagnosticated by another physician. At the begining 7 had only respiratory symptoms. Five patients were amlnurished. Sputum culture were positive in 3 patients, 2 had Pseudomona aeruginosa, 1 had Streptococo alfa hemolitic and Moraxella catarrhalis. Sweat test were nor done by pilocarpine test, we used a non standarized method; only one patient had 52 mEq/L, the other were above 60 mEq/L of chloride. (Rev Med Hered 1994; 5: 204-208).