The European chILD-EU register has developed standardized protocols for diagnosis and therapy. These will continuously be improved. Moreover, the register will promote scientific-clinical research. Patients included into the register are offered a peer review by international experts for confirmation of the initial diagnosis.
The primary goal of the European chILD-EU register and biobank are the long-term recording and conservation of data and biomaterials from as many cases with rare children’s interstitial lung diseases (chILD).
Physicians interested in including patients in the register should fill in the registration form.
Cooperation and input into these activities are very welcomed!