Abstract
We report 13-year old boy with a chronic pseudomonas bronchitis who was first diagnosed as having cystic fibrosis at this age because of an elevated sweat chloride employing pilocarpine-iontophoresis. He is heterozygote for the gene mutation Delta F508. We point out the often moderate course of illness in compound heterozygotes.
| Translated title of the contribution | A 13-year old boy with a mild form of cystic fibrosis and heterozygote gene mutation for delta F508 |
|---|---|
| Original language | German |
| Journal | Pneumologie |
| Volume | 45 |
| Issue number | 11 |
| Pages (from-to) | 910-912 |
| Number of pages | 3 |
| ISSN | 0934-8387 |
| Publication status | Published - 1991 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 5 Gender Equality
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SDG 10 Reduced Inequalities
Research Areas and Centers
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)
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