Torg-Winchester syndrome (Q98289)
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Winchester syndrome is a hereditary disorder characterised by extremely short stature, coarse face, corneal opacities, generalised osteolysis and progressive painful arthropathy with joint stiffness and contractures of distal phalanges in combination with skin changes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1076780824 |
||
| English | Torg-Winchester syndrome |
Winchester syndrome is a hereditary disorder characterised by extremely short stature, coarse face, corneal opacities, generalised osteolysis and progressive painful arthropathy with joint stiffness and contractures of distal phalanges in combination with skin changes. |
Statements
CID11:ID_1076780824
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dki-india-ID_1076780824
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Concluído
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15 August 2026
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