The prospective juvenile systemic sclerosis inceptions cohort – http://www.juvenile-scleroderma.com
نویسندگان
چکیده
Address: 1Hamburger Zentrum für Kinderund Jugendrheumatologie, Hamburg, Germany, 2Pediatric Rheumatology, University Children's Hospital, Barcelona, Spain, 3Pediatric Rheumatology, University Children's Hospital, Sydney, Australia, 4Pediatric Rheumatology, University Children's Hospital, Liverpool, UK, 5Pediatric Rheumatology, University Children's Hospital, Columbus, USA, 6Pediatric Rheumatology, University Children's Hospital, New York, USA, 7Pediatric Rheumatology, University Children's Hospital, Sao Paolo, Brazil, 8Pediatric Rheumatology, GOS, London, UK, 9Pediatric Rheumatology, University Children's Hospital, Los Angeles, USA, 10Pediatric Rheumatology, University Children's Hospital, Buenos Aires, Argentina and 11Pediatric Rheumatology, University Children's Hospital, Padua, Italy * Corresponding author
منابع مشابه
Update on the juvenile systemic sclerosis inception cohort http://www.juvenile-scleroderma.com
Results We report the patient characteristics at time point 0, 6 and 12 months of their follow up. We present date on 25 patients. The mean follow up of the patients in the cohort are 3.5 years. No patient died during the follow up. Eighteen of the 25 patients were female. The mean age of the onset of Raynaud symptomatic was 10.4 years, the youngest patient was 2.0 years of age. The mean age at...
متن کاملسندرم شبه اسکلرودرمی معرفی یک بیمار نادر (سندرم ورنر)
Scleroderma-like syndromes are a group of disorders that mimic systemic sclerosis. Werner’s syndrome is a genetically inherited syndrome that can be misdiagnosed as systemic scleroderomia. The syndrome is charachterized by sclerosis or stiffening of the skin, progeris, bilatera l juvenile cataract, endocrinopathies, premature coronary artery disease, alopecia, nail plate changes, hyperpigmentat...
متن کاملAnticardiolipin Antibodies in Juvenile Rheumatoid Arthritis and Systemic Lupus Erythematosus
Background: Antiphospholipid antibody syndrome (APS) can either occur as a primary syndrome or associated with other autoimmune diseases such as systemic lupus erythematosus (SLE). Anticardiolipin antibody (aCL) of IgG and/or IgM isotype in blood, measured by a standardized ELISA is the most acceptable laboratory criteria. APS IgG isotype, particularly IgG2 subclass is more strongly associated ...
متن کاملStem cell transplantation for rheumatic autoimmune diseases
Immunoablative therapy and hematopoietic stem cell transplantation (HSCT) is an intensive treatment modality aimed at 'resetting' the dysregulated immune system of a patient with immunoablative therapy and allow outgrowth of a nonautogressive immune system from reinfused hematopoietic stem cells, either from the patient (autologous HSCT) or a healthy donor (allogeneic HSCT). HSCT has been shown...
متن کاملNew insights into the pathogenesis and management of juvenile systemic sclerosis
2015 Systemic sclerosis remains one of the most clinically challenging diseases for rheumatologists and patients continue to suffer from a considerable degree of morbidity and mortality. Even though the pathogenesis of the disease remains complex and poorly understood, new research over the past several years have brought us closer to an understanding of the underlying disease mechanisms and co...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 6 شماره
صفحات -
تاریخ انتشار 2008