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Diagnostik der cystischen Fibrose

  • Chapter
Cystische Fibrose

Zusammenfassung

Klinische Symptome sind unverändert Hauptgründe, an eine CF zu denken. Auch wenn sich die Möglichkeiten der Diagnostik in den letzten Jahrzehnten verbessert haben, wird die CF bei vielen Kindern immer noch nicht rechtzeitig erkannt. Dies liegt vor allem daran, dass Symptome nicht als hinweisend auf die Erkrankung angesehen und die entsprechenden diagnostischen Testverfahren, wie die Bestimmung der Natrium- und Chloridkonzentration im Schweiß, nicht eingesetzt werden. In Abwesenheit eines sicheren und flächendeckenden Neugeborenenscreenings sind es die klinischen Zeichen, die den betreuenden Arzt an die Erkrankung denken lassen müssen und zur Einleitung der weiteren Diagnostik führen sollten. Für die verschiedenen Organsysteme sei vor allem auch auf die detaillierten Darstellungen im Teil Organspezifische Aspekte verwiesen

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  1. Kinderklinik und Poliklinik im Dr. von Haunerschen Kinderspital der Ludwig-Maximilians-Universität, Lindwurmstr. 4, 80337, München, Deutschland

    Dietrich Reinhardt

  2. Abteilung für Kinder- und Jugendheilkunde, Wilhelminenspital der Stadt Wien, Montlearstr. 37, 1171, Wien, Österreich

    Manfred Götz

  3. Inselspital, Medizinische Universitäts-Kinderklinik, Freiburgstr. 23, 3010, Bern, Schweiz

    Richard Kraemer  & Martin H. Schöni  & 

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Eichler, I. et al. (2001). Diagnostik der cystischen Fibrose. In: Reinhardt, D., Götz, M., Kraemer, R., Schöni, M.H. (eds) Cystische Fibrose. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56796-4_5

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