Familial osteochondritis dissecans (Q95286): Difference between revisions
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A osteocondrite dissecante familiar é um transtorno esquelético genético raro. Ela se caracteriza clinicamente pelo desenvolvimento condro-esquelético anormal, com estatura desproporcionalmente baixa e deformidades esqueléticas que afetam preferencialmente os joelhos, quadris, tornozelos e cotovelos. Ela se inicia geralmente no final da infância ou na adolescência. | |||
| description / en | description / en | ||
Familial osteochondritis dissecans is a rare genetic skeletal disorder characterised clinically by abnormal chondro-skeletal development, disproportionate short stature and skeletal deformation mainly affecting the knees, hips, ankles and elbows with onset generally in late childhood or adolescence. | |||
Revision as of 11:01, 16 August 2026
Familial osteochondritis dissecans is a rare genetic skeletal disorder characterised clinically by abnormal chondro-skeletal development, disproportionate short stature and skeletal deformation mainly affecting the knees, hips, ankles and elbows with onset generally in late childhood or adolescence.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_117325330 |
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| English | Familial osteochondritis dissecans |
Familial osteochondritis dissecans is a rare genetic skeletal disorder characterised clinically by abnormal chondro-skeletal development, disproportionate short stature and skeletal deformation mainly affecting the knees, hips, ankles and elbows with onset generally in late childhood or adolescence. |
