Physicians significantly underestimated the proportion of patients with systemic sclerosis who experienced pain, with rates of 43.4% vs 96.0%.

Both systemic sclerosis and systemic lupus erythematosus have down-regulated RGS5, but they also have distinctive genetic ...

She was 44 when she was diagnosed with systemic scleroderma," he told NIH Medline Plus Magazine in 2019. "She got treatment, but it was just treating her symptoms with drugs like prednisone and ...

Scleroderma is an autoimmune disease, which means that the body’s immune system attacks itself. Scleroderma involves the hardening and tightening of the skin and connective tissues. It has two forms; ...

She was 44 when she was diagnosed with systemic scleroderma. She passed away just two years later,” he told “NIH Medline Plus Magazine” in 2019.

She was 44 in 1992 when she was diagnosed with systemic scleroderma, a disease that strikes mostly women in the prime of their lives. She had been living in Bucks County, Pennsylvania, but moved ...

“In systemic sclerosis, the gastrointestinal tract is incredibly important to understand,” Tracy M. Frech, MD, MS, director of the Systemic Sclerosis Clinic and director of clinical trials for ...

Puffy hands and fingers, as well as other symptoms, can precede the “warning sign” of Raynaud’s syndrome as the initial ...

Systemic sclerosis (SSc) sine scleroderma (ssSSc) was proposed as a distinct disease subtype in 1986, but no data were published to support a separate classification. [3] ...

The Dietz team's results are described in the Oct. 10 issue of Nature. Patients with systemic sclerosis, also known as systemic scleroderma, experience a sudden hardening, or fibrosis, of the skin.

Systemic sclerosis is an independent determinant for moderate to severe coronary calcification or atherosclerosis, suggests a new study. Conventional cardiovascular risk factors such as age and ...