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Systemic sclerosis (scleroderma)
1991Estimating prognosis in systemic sclerosis is particularly difficult for a number of reasons. First, it is a disorder of remarkable clinical heterogeneity. Patients may be classified as having diffuse (widespread) or limited (restricted) cutaneous involvement. Additional variants not yet described are likely to exist.
Virginia D. Steen, Thomas A. Medsger
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Scleroderma (Systemic Sclerosis) [PDF]
Scleroderma is a systemic disease characterized by progressive fibrosis of the skin and multiple organs. The term “scleroderma” means literally “hard skin”
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Systemic Sclerosis (Scleroderma)
Archives of Dermatology, 1986This book is based on the proceedings of the International Conference on Scleroderma held in Austin, Tex in 1981. The coverage is encyclopedic, ranging from history to animal models, epidemiology to therapy. The individual chapters are in brief report format with useful references.
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Systemic manifestations in localized scleroderma
Current Rheumatology Reports, 2004In this paper, the various systemic manifestations reported in localized scleroderma, their incidence, their relationship with systemic sclerosis, and their relationship with other autoimmune or connective tissue diseases will be analyzed.
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1999
Abstract The next two chapters will deal with the systemic forms of scleroderma, both diffuse and, as well as scleroderma sine sclerosis, in which there is internal organ involvement but no thickening of the skin (sine means without and sclerosis means hardening). The term systemic means that this form of scleroderma affects the internal
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Abstract The next two chapters will deal with the systemic forms of scleroderma, both diffuse and, as well as scleroderma sine sclerosis, in which there is internal organ involvement but no thickening of the skin (sine means without and sclerosis means hardening). The term systemic means that this form of scleroderma affects the internal
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Systemic and localized scleroderma in children
Current Opinion in Rheumatology, 1996All forms of scleroderma are rare in childhood. The most common form in childhood is localized scleroderma, which may take the form of morphea or linear scleroderma. Localized scleroderma is often benign but may cause significant deformity if it occurs on the face or extends across joint surfaces. Progressive systemic sclerosis is much less frequent in
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Caring for the Patient With Limited Systemic Scleroderma
Orthopedic Nursing, 2016Kelly Denise Lachner
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Scleroderma in Children and Adolescents: Localized Scleroderma and Systemic Sclerosis.
The Pediatric clinics of North America, 2018Suzanne C. Li
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