Reynolds syndrome (Q91003): Difference between revisions
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A síndrome de Reynolds é uma doença autoimune rara, que consiste na combinação de cirrose biliar primária e esclerose sistêmica. Em alguns pacientes, esta síndrome também foi associada à síndrome de Sjögren e à anemia hemolítica. As características clínicas típicas incluem icterícia, níveis sanguíneos elevados de fosfatase alcalina, calcinose cutânea, telangiectasia e prurido. | |||
| description / en | description / en | ||
Reynolds syndrome is a rare autoimmune disease, consisting of the combination of primary biliary cirrhosis and systemic sclerosis. In some patients this syndrome has also been associated with Sjögren syndrome and haemolytic anaemia. Typical clinical features include jaundice, elevated blood levels of alkaline phosphatase, calcinosis cutis, telangiectasia and pruritus. | |||
Revision as of 17:59, 15 August 2026
Reynolds syndrome is a rare autoimmune disease, consisting of the combination of primary biliary cirrhosis and systemic sclerosis. In some patients this syndrome has also been associated with Sjögren syndrome and haemolytic anaemia. Typical clinical features include jaundice, elevated blood levels of alkaline phosphatase, calcinosis cutis, telangiectasia and pruritus.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1409844299 |
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| English | Reynolds syndrome |
Reynolds syndrome is a rare autoimmune disease, consisting of the combination of primary biliary cirrhosis and systemic sclerosis. In some patients this syndrome has also been associated with Sjögren syndrome and haemolytic anaemia. Typical clinical features include jaundice, elevated blood levels of alkaline phosphatase, calcinosis cutis, telangiectasia and pruritus. |
