نتایج جستجو برای: limited systemic scleroderma

تعداد نتایج: 596253  

Journal: :Reumatologia clinica 2007
María Luisa Velloso Feijoo Sergio Rodríguez Montero Paz González Moreno Lucía Mayordomo González Eduardo Rejón Gieb Jorge Fernández Alonso José Luis Marenco de La Fuente

The renal affectation is infrequent in scleroderma, unlike other collagen diseases. The appearance of nephrotic syndrome has been related to the drug use, specially the D-penicilamine, or rarely as a manifestation of secondary amilodosis, quite infrequent in scleroderma. We report a case of nephrotic syndrome in a patient with systemic scleroderma, produced by a membranous glomerulonephritis, e...

Journal: :Drugs 2001
C Leighton

Scleroderma or systemic sclerosis is a rare condition with many clinical manifestations including Raynaud's phenomenon. As with many other rarely encountered diseases, drug therapy for scleroderma is often empirical with little evidence in the form of randomised controlled trials to aid drug choice. Raynaud's phenomenon has been recognised for well over 100 years. A considerable number of clini...

2018

Systemic sclerosis (SSc) is a multisystem autoimmune disease in which there is increased fibroblast activity resulting in abnormal growth of connective tissue. This causes vascular damage and fibrosis. Fibrosis occurs in skin, the gastrointestinal (GI) tract, heart, lungs and other internal organs. Vascular manifestations include secondary Raynaud's phenomenon, ischaemia of extremities, pulmona...

Behzad Dehghani, Javad Moayedi, Mohammad Ali Nazarinia, Tayebeh Hashempour, Zahra Hasanshahi, Zahra Musavi,

Background: Scleroderma is a chronic systemic disorder that affects the connective tissues. It is characterized by several immune manifestations, inflammation, vascular damage, and fibrosis. Some of the viral infections with complex mechanisms are involved in the development and progression of many autoimmune diseases, such as scleroderma. The present study aimed to investigate the serological ...

2013
Awa Oumar Touré Fatimata Ly Abibatou Sall Alassane Diatta Macoura Gadji Moussa Seck Blaise Faye Tandakha Dieye Saliou Diop

OBJECTIVE Antiphospholipid antibodies (APLs) could be associated with an increased risk of vascular pathologies in systemic scleroderma. The aim of our study was to search for APLs in patients affected by systemic scleroderma and to evaluate their involvement in the clinical manifestations of this disease. MATERIALS AND METHODS We conducted a cross-sectional descriptive study, from January 20...

Journal: :The Journal of clinical investigation 1979
J Uitto E A Bauer A Z Eisen

To assess potential abnormalities in collagen metabolism in systemic scleroderma, skin fibroblast lines from patients with this disease were established and compared to control cell lines derived from healthy subjects. For studies on the biosynthesis of procollagen, the cells were incubated with [(14)C]proline in a medium supplemented with ascorbic acid and beta-aminopropionitrile, and the synt...

2012

While it is called by many names and comes in different varieties, SScl is characterized by one basic problem: overproduction of collagen. Collagen is an important protein in the body that is a component of scar tissue, which allows injuries to heal. When too much collagen is deposited, however, a number of problems can arise, and this is the basic obstacle that must be faced in patients with S...

2017

Systemic sclerosis (SSc) is a multisystem autoimmune disease in which there is increased fibroblast activity resulting in abnormal growth of connective tissue. This causes vascular damage and fibrosis. Fibrosis occurs in skin, the gastrointestinal (GI) tract, heart, lungs and other internal organs. Vascular manifestations include secondary Raynaud's phenomenon, ischaemia of extremities, pulmona...

Journal: :Reumatologia clinica 2009
Zoilo Morel Eduardo Benadón Enrique Faugier María Del Rocío Maldonado

INTRODUCTION Scleroderma is an autoimmune disease that involves the connective tissue characterized by skin fibrosis, classified as localized and systemic (participation of one or more internal organs). The primary objective of this study is to describe and analyze the clinical and laboratory findings in a group of children diagnosed with scleroderma at a referral hospital. MATERIAL AND METHO...

2004
Panayiotis G. Vlachoyiannopoulos Haralampos M. Moutsopoulos

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