Хвороба Тімана, сімейна форма
ORPHA:3314· ICD-10 M93.2· Thiemann disease, familial form
Визначення(English summary)
A very rare genetic necrotic bone disorder characterized 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.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Not applicable
- Вік початку
- Adolescent