Distal arthrogryposis type 3 (Q104860): Difference between revisions
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16 August 2026
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Latest revision as of 10:43, 17 August 2026
Distal arthrogryposis type 3 (aka Gordon Syndrome) is an extremely rare genetic disorder that is characterised by the combination of camptodactyly (a permanent fixation of several fingers in a flexed position), clubfoot or talipes (abnormal bending inward of the foot), and, in 25 % of patients, cleft palate. Intelligence is normal but in some cases, additional abnormalities (for example, scoliosis and cryptorchidism) may also be present.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1444357813 |
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| English | Distal arthrogryposis type 3 |
Distal arthrogryposis type 3 (aka Gordon Syndrome) is an extremely rare genetic disorder that is characterised by the combination of camptodactyly (a permanent fixation of several fingers in a flexed position), clubfoot or talipes (abnormal bending inward of the foot), and, in 25 % of patients, cleft palate. Intelligence is normal but in some cases, additional abnormalities (for example, scoliosis and cryptorchidism) may also be present. |
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CID11:ID_1444357813
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dki-india-ID_1444357813
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Concluído
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16 August 2026
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