Torg-Winchester syndrome (Q98289): Difference between revisions
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Revision as of 14:41, 16 August 2026
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 |
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| default for all languages | ID_1076780824 |
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| 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. |
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CID11:ID_1076780824
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dki-india-ID_1076780824
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