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    D110H Mutation

    Thank u! Wish u and your daughter the very best. I hope thay will stay asymptomatic forever
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    D110H Mutation

    I am happy for you. Unfortunately Kalydeco is not approved in my country. Do you know any other children/adults who have the same mutation? I am interested how people who are not taking Kalydeco are feeling?
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    D110H Mutation

    How is she? Has she developed any of the symptomes?
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    D110H Mutation

    Hello everyone! My daughter was diagnosed with CF- D110H and other very rare mutation of I class through prenatal screening. She has boarderline sweat test results. Is 9 months old with no clinical symptoms. Has never been ill. Does anyone have the same D110 H mutation ?
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