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Scleroderma is a group of autoimmune diseases that may result in changes to the skin, blood vessels, muscles, and internal organs. [2] [6] [8] The disease can be either localized to the skin or involve other organs, as well. [2] Symptoms may include areas of thickened skin, stiffness, feeling tired, and poor blood flow to the fingers or toes ...
Systemic scleroderma, or systemic sclerosis, is an autoimmune rheumatic disease characterised by excessive production and accumulation of collagen, called fibrosis, in the skin and internal organs and by injuries to small arteries. There are two major subgroups of systemic sclerosis based on the extent of skin involvement: limited and diffuse.
Morphea is a form of scleroderma that mainly involves isolated patches of hardened skin on the face, hands, and feet, or anywhere else on the body, usually with no internal organ involvement. [1] However, in Deep Morphea inflammation and sclerosis can be found in the deep dermis, panniculus, fascia, superficial muscle and bone.
Scleroderma citrinum. Scleroderma citrinum, commonly known as the common earthball, [1] pigskin poison puffball, [2] or common earth ball, [3] is the most common species of earthball fungus in the UK and occurs widely in woods, heathland and in short grass from autumn to winter. Scleroderma citrinum has two synonyms, Scleroderma aurantium ...
CREST syndrome, also known as the limited cutaneous form of systemic sclerosis (lcSSc), is a multisystem connective tissue disorder. The acronym "CREST" refers to the five main features: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia. [2]
Scleroderma echinosporites Rouse (1962) Scleroderma endoxanthum Petch (1919) Scleroderma flavidum Ellis & Everh. (1885) Scleroderma floridanum Guzmán (1967) Scleroderma franceschii Macchione (2000) [4] Scleroderma furfurellum Zeller (1947) Scleroderma guzmanii Ortiz-Rivero, Watling, Guzm.-Dáv.
Scleromyositis, is an autoimmune disease (a disease in which the immune system attacks the body). People with scleromyositis have symptoms of both systemic scleroderma and either polymyositis or dermatomyositis, and is therefore considered an overlap syndrome. Although it is a rare disease, it is one of the more common overlap syndromes seen in ...
The Scleroderma Research Foundation ( SRF) is a non-profit organization based in San Francisco that funds research into scleroderma. The SRF also funds and supports Scleroderma Centers of Excellence, including the Johns Hopkins Hospital 's Scleroderma Center in Baltimore . Over 30 years, the SRF has raised millions of dollars for scleroderma ...
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