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- W2563851810 abstract "Abstract Systemic scleroderma (SSc) is a multisystem disease with microvascular abnormalities, autoimmune disorders, excessive collagen production and deposition, and fibrosis of the skin and internal organs. According to the simplest, though incomplete classification, there are two forms of SSc: diffuse and limited (formerly acrosclerosis). CREST syndrome is a subtype of limited SSc, characterized by: calcinosis, Raynaud’s phenomenon, esophageal dysfunction, sclerodactyly, and telangiectasia. We present a patient with all the features of the CREST syndrome, which appeared at the age of 43 and lasted for 23 years. The patient presented with a gradual development of symptoms during the first ten years, from Raynaud’s phenomenon, skin sclerosis, calcinosis, telangiectasia, and esophageal dysmotility. The diagnosis was based on clinical findings and relevant diagnostic procedures. The article presents a literature review on the epidemiology, etiology, pathophysiology, clinical manifestations, various attempts at classification, diagnostic criteria, and therapeutic modalities. When classifying systemic scleroderma into two main types — diffuse and limited, with CREST syndrome as a variant of the latter, it should be pointed out that both types represent clinical forms of systemic sclerosis, share similar visceral involvement, laboratory abnormalities and course which is variable, as was the case in our patient." @default.
- W2563851810 created "2017-01-06" @default.
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- W2563851810 creator A5069140179 @default.
- W2563851810 creator A5080202166 @default.
- W2563851810 date "2015-09-01" @default.
- W2563851810 modified "2023-09-26" @default.
- W2563851810 title "CREST Syndrome - a Limited Form of Systemic Scleroderma: a Case Report and Literature Review" @default.
- W2563851810 cites W121967502 @default.
- W2563851810 cites W159804607 @default.
- W2563851810 cites W1600950849 @default.
- W2563851810 cites W160816747 @default.
- W2563851810 cites W1712086269 @default.
- W2563851810 cites W17148415 @default.
- W2563851810 cites W1808798629 @default.
- W2563851810 cites W1830406618 @default.
- W2563851810 cites W1963840039 @default.
- W2563851810 cites W1967028030 @default.
- W2563851810 cites W1967654015 @default.
- W2563851810 cites W1971029753 @default.
- W2563851810 cites W1972177298 @default.
- W2563851810 cites W1977625417 @default.
- W2563851810 cites W1978157635 @default.
- W2563851810 cites W1979082115 @default.
- W2563851810 cites W1979493555 @default.
- W2563851810 cites W1979860433 @default.
- W2563851810 cites W1983750629 @default.
- W2563851810 cites W1991888712 @default.
- W2563851810 cites W1996971331 @default.
- W2563851810 cites W1998280922 @default.
- W2563851810 cites W2000887725 @default.
- W2563851810 cites W2001101579 @default.
- W2563851810 cites W2001452538 @default.
- W2563851810 cites W2002457445 @default.
- W2563851810 cites W2005406074 @default.
- W2563851810 cites W2008733275 @default.
- W2563851810 cites W2010584977 @default.
- W2563851810 cites W2011509783 @default.
- W2563851810 cites W2014150714 @default.
- W2563851810 cites W2015031838 @default.
- W2563851810 cites W2015375716 @default.
- W2563851810 cites W2026535970 @default.
- W2563851810 cites W2038761836 @default.
- W2563851810 cites W2039816156 @default.
- W2563851810 cites W2056351738 @default.
- W2563851810 cites W2065938351 @default.
- W2563851810 cites W2072708404 @default.
- W2563851810 cites W2074982867 @default.
- W2563851810 cites W2085090195 @default.
- W2563851810 cites W2086737296 @default.
- W2563851810 cites W2089255535 @default.
- W2563851810 cites W2091867969 @default.
- W2563851810 cites W2092408485 @default.
- W2563851810 cites W2100137363 @default.
- W2563851810 cites W2101295768 @default.
- W2563851810 cites W2104276638 @default.
- W2563851810 cites W2105297145 @default.
- W2563851810 cites W2105493742 @default.
- W2563851810 cites W2105605672 @default.
- W2563851810 cites W2107847924 @default.
- W2563851810 cites W2110062760 @default.
- W2563851810 cites W2111374061 @default.
- W2563851810 cites W2112067379 @default.
- W2563851810 cites W2112162481 @default.
- W2563851810 cites W2115561534 @default.
- W2563851810 cites W2117516392 @default.
- W2563851810 cites W2120317399 @default.
- W2563851810 cites W2120901067 @default.
- W2563851810 cites W2121599003 @default.
- W2563851810 cites W2122131766 @default.
- W2563851810 cites W2126139459 @default.
- W2563851810 cites W2126259139 @default.
- W2563851810 cites W2128919501 @default.
- W2563851810 cites W2129244767 @default.
- W2563851810 cites W2137056396 @default.
- W2563851810 cites W2138453392 @default.
- W2563851810 cites W2144578575 @default.
- W2563851810 cites W2151470207 @default.
- W2563851810 cites W2151558035 @default.
- W2563851810 cites W2152517606 @default.
- W2563851810 cites W2152917175 @default.
- W2563851810 cites W2158879607 @default.
- W2563851810 cites W2160494189 @default.
- W2563851810 cites W2161359743 @default.
- W2563851810 cites W2161543010 @default.
- W2563851810 cites W2163978696 @default.
- W2563851810 cites W2164566731 @default.
- W2563851810 cites W2166652139 @default.
- W2563851810 cites W2168198817 @default.
- W2563851810 cites W2218752636 @default.
- W2563851810 cites W2299513640 @default.
- W2563851810 cites W2394768513 @default.
- W2563851810 cites W2410028301 @default.
- W2563851810 cites W2413748689 @default.
- W2563851810 cites W2415716633 @default.