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In contrast to the common perception that lung function declines faster early in the course of scleroderma-associated interstitial lung disease and plateaus several years after diagnosis, we show that patients have distinct patterns of lung function decline that remain relatively consistent during long-term follow-up.

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This page is a summary of: Does Systemic Sclerosis–associated Interstitial Lung Disease Burn Out? Specific Phenotypes of Disease Progression, Annals of the American Thoracic Society, December 2018, American Thoracic Society,
DOI: 10.1513/annalsats.201806-362oc.
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