Torg-Winchester syndrome (Q98289): Difference between revisions
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A síndrome de Winchester é um transtorno hereditário caracterizado por estatura extremamente baixa, face grosseira, opacidades da córnea, osteólise generalizada e artropatia dolorosa progressiva com rigidez articular e contraturas de falanges distais em combinação com alterações cutâneas. | |||
| description / en | description / en | ||
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. | |||
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 |
|---|---|---|---|
| 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. |
