Thiemann disease, familial form (Q95264): Difference between revisions
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A doença de Thiemann é um transtorno ósseo necrosante genético, muito raro, caracterizado clinicamente pela presença de edema indolor das articulações interfalângicas proximais e osteonecrose de epífises, que evolui para o desenvolvimento de alterações de osteoartrite. Ela se inicia antes dos 25 anos de idade e frequentemente tem uma evolução benigna. | |||
| description / en | description / en | ||
Thiemann disease is a very rare genetic necrotic bone disorder characterised clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course. | |||
Revision as of 10:59, 16 August 2026
Thiemann disease is a very rare genetic necrotic bone disorder characterised clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_67016273 |
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| English | Thiemann disease, familial form |
Thiemann disease is a very rare genetic necrotic bone disorder characterised clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course. |
