Juvenile hyaline fibromatosis (Q101615): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1890146024 / rank | |||
Normal rank | |||
Revision as of 18:27, 16 August 2026
Juvenile hyaline fibromatosis (JHF) is a genetic condition characterised by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints due to perivascular hyaline deposition. Typical diagnostic criteria are multiple hyaline subcutaneous fibroma, filamentous tumours of the skin, gingival fibromatosis, muscle contractures of the extremities and multiple osteolytic bone destructions.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1890146024 |
||
| English | Juvenile hyaline fibromatosis |
Juvenile hyaline fibromatosis (JHF) is a genetic condition characterised by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints due to perivascular hyaline deposition. Typical diagnostic criteria are multiple hyaline subcutaneous fibroma, filamentous tumours of the skin, gingival fibromatosis, muscle contractures of the extremities and multiple osteolytic bone destructions. |
