Of note, a significantly longer time interval from RP onset to SSc diagnosis was observed either in ssSSc and lcSSc compared with dcSSc, as well as an increasing trend in DU rates through the three subsets (ssSSc<lcSSc<dcSSc).
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Systemic sclerosis sine scleroderma: clinical and serological features and relationship with other cutaneous subsets in a large series of patients from the national registry 'SPRING' of the Italian Society for Rheumatology.
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