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. | |||||||||||||||
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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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1076780824 / rank | |||||||||||||||
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CID11:ID_1076780824 | |||||||||||||||
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dki-india-ID_1076780824 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1076780824 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest 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. |
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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