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Interstitial lung disease in children – genetic background and associated phenotypes

Dominik Hartl email and Matthias Griese email

Pediatric Pneumology, Childrens' hospital of the Ludwig-Maximilians-University, Munich, Germany

author email corresponding author email

Respiratory Research 2005, 6:32doi:10.1186/1465-9921-6-32

Published: 8 April 2005

Additional files

Additional File 1:

Table 1. Pathological features and clinical phenotypes of reported cases with partial SP-B deficiency. Table 2. Pathological features and clinical phenotypes of reported cases with mutations in the SP-C gene. Table 3. Overview: Pediatric interstitial lung disease associated with surfactant protein deficiency or ABCA3 mutations

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