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EIN 13 JAHRIGER JUNGE MIT EINER MILDEN FORM DER ZYSTISCHEN FIBROSE UND HETEROZYGOTER GENMUTATION FUR DELTA F508

Translated title of the contribution: A 13-year old boy with a mild form of cystic fibrosis and heterozygote gene mutation for delta F508

O. Hiort, A. Artlich, W. Wiebicke

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 contributionA 13-year old boy with a mild form of cystic fibrosis and heterozygote gene mutation for delta F508
Original languageGerman
JournalPneumologie
Volume45
Issue number11
Pages (from-to)910-912
Number of pages3
ISSN0934-8387
Publication statusPublished - 1991

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 5 - Gender Equality
    SDG 5 Gender Equality
  3. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities

Research Areas and Centers

  • Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)

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