Belgian Genetic Tests database
Jackson-Weiss syndrome
| Name: |
Jackson-Weiss syndrome
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| Description: |
Jackson-Weiss syndrome (JWS) is a rare genetic disorder characterized by foot malformations (tarsal and metatarsal fusions; short, broad, medially deviated great toes) and in some patients craniosynostosis with facial anomalies. Hands are normal in affected patients.
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| ORPHAcode: |
1540
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| Synonyms: |
Craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome
JWS
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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