Reynolds syndrome (Q91003): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_1409844299 | |||
| Property / CURIE: CID11:ID_1409844299 / rank | |||
Normal rank | |||
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 |
||
| 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. |
Statements
CID11:ID_1409844299
0 references
