Mevalonate kinase deficiency with recurrent fever (Q88717): Difference between revisions
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A deficiência de mevalonato quinase [MVK] com febre recorrente, com ou sem hiper -IgD, é uma doença autoinflamatória associada a mutações no gene mevalonato quinase. Isso resulta em crises de inflamação na forma de febre, linfadenopatia, baço aumentado e serosite, associado com aumento de reagentes de fase aguda. | |||
| description / en | description / en | ||
Mevalonate kinase [MVK] deficiency with recurrent fever, with or without hyperIgD, is an autoinflammatory disease associated with mutations in the mevalonate kinase gene. This results in clinical attacks of inflammation in the form of fever, lymphadenopathy, enlarged spleen and serositis along with increased acute phase reactants. | |||
Revision as of 15:06, 15 August 2026
Mevalonate kinase [MVK] deficiency with recurrent fever, with or without hyperIgD, is an autoinflammatory disease associated with mutations in the mevalonate kinase gene. This results in clinical attacks of inflammation in the form of fever, lymphadenopathy, enlarged spleen and serositis along with increased acute phase reactants.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_910632716 |
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| English | Mevalonate kinase deficiency with recurrent fever |
Mevalonate kinase [MVK] deficiency with recurrent fever, with or without hyperIgD, is an autoinflammatory disease associated with mutations in the mevalonate kinase gene. This results in clinical attacks of inflammation in the form of fever, lymphadenopathy, enlarged spleen and serositis along with increased acute phase reactants. |
