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Thiemann disease, familial form

ORPHA:3314· ICD-10 M93.2

Definition

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.

Prevalence
<1 / 1 000 000
Inheritance
Not applicable
Age of onset
Adolescent