Maladie de DupuytrenSummary The prevalence of Raynaud's syndrome, of arterial calcifications and of Dupuytren's contracture was studied in 155 subjects of both sexes, decade by decade from 20 to 90 years. Moreover the force of prehension and two-point discrimination were measured separately. The...
We present the main clinical features and prognosis of syndromes associated with antibodies antisynthetase groupe, emphasizing the anti-Jo1. Method: The antisynthetase syndrome is a subgroup of idiopathic inflammatory myopathies, characterized by interstitial lung disease, arthritis, Raynaud's phenomenon ...
Such patients may be asymptomatic, may have oral thrush and recurrent infections, or may develop autoimmune disease such as juvenile idiopathic arthritis, immune thrombocytopenic purpura, and Raynaud phenomenon. Approximately 1% of DGS patients have “complete DGS”, with absence of circulating T cells...
Raynaud phenomenon, usually mild, can be observed in nearly 30% of patients with primary SS.1 Pulmonary Involvement Although common, pulmonary involvement is seldom clinically significant in patients with SS.2 Cough is often the main respiratory symptom and is usually a symptom of xerotrachea. ...
Raynaud's phenomenon was observed in 22 (33.33%) patients with ILD, which was a significantly higher rate compared to those without (5.99%, p < 0.001). Haematological involvement was the main extraglandular manifestation of patients with ILD (46 out of 66 patients [69.70%]). Twenty-six...
Raynaud’s phenomenon is usually the first symptom and is followed years later by skin thickening of the hands (sclerodactyly) as well as the other manifestations of the disease. Systemic involvement (e.g., lung fibrosis and kidney failure) tends to be less severe than in systemic sclerosis....
Penisson-Besnier I, Lebouvier T, Moizard MP, Ferre M, Barth M, Marc G, Raynaud M, Bonneau D: Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndrome. Am J Med Genet A. 2008, 146A: 464-467. 10.1002/ajmg.a.32154. Article CAS PubMed Google Scholar Cureton ...
Budny B, Chen W, Omran H, Fliegauf M, Tzschach A, Wisniewska M, Jensen LR, Raynaud M, Shoichet SA, Badura M, Lenzner S, Latos-Bielenska A, Ropers HH: A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital ...
A Letamendia, J López-Román, J Bustamante-Munguira, J Herreros Digital periarterial sympathectomy in the management of post-traumatic Raynaud syndrome J Vasc Surg, 63 (2) (2016), pp. 459-465 Google Scholar Cited by (0)The standard therapy for thrombotic antiphospholipid syndrome (APS) is...
36 Tao, J., Van Esch, H., Hagedorn-Greiwe, M., Hoffmann, K., Moser, B., Raynaud, M. et al. Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation. Am. J. Hum. Genet. 75, 1149–1154 (2004). 37 ...