Introduction to Rhupus Syndrome
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Rhupus syndrome is a rare and incompletely described autoimmune entity in which the same patient sequentially develops symptoms both of Rheumatoid Arthritis (RA) and Systemic Lupus Erythematosus (SLE).
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Rhupus syndrome was diagnosed.
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Rhupus syndrome: Assessment of its prevalence and its clinical and instrumental characteristics in a prospective cohort of 103 SLE patients.
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Rhupus syndrome is a clinical condition characterized by a combination of the clinical and immunologic features of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) (1).
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Such condition defines the Rhupus syndrome, which is a rare overlapping syndrome.
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Organ involvement in Rhupus syndrome is relatively rare.
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Rhupus syndrome is a rare clinical condition, characterized by overlap of SLE and RA.
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However, to date, no consensus exists on how to define the rhupus syndrome.
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Rhupus syndrome, a rare entity, is the co-existence of systemic lupus erythematosus (SLE) with rheumatoid arthritis (RA).
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Interstitial lung disease (ILD) is seen in 17% of patients with Rhupus syndrome.
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To the Editor,Occasionally, we encounter patients who develop overlapping features of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE), which is termed as ‘rhupus syndrome’ [1].
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In less than 15% of patients, joints may be more severely affected by deforming (Jaccoud's arthropathy) and/or erosive arthropathy (Rhupus syndrome).
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