Baller-Gerold syndrome (Q93984): Difference between revisions
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15 August 2026
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Latest revision as of 09:05, 16 August 2026
Baller-Gerold syndrome is an autosomal recessive disorder characterised by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius). Patients have a predisposition to cancer, in particular osteosarcoma. B
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1650688177 |
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| English | Baller-Gerold syndrome |
Baller-Gerold syndrome is an autosomal recessive disorder characterised by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius). Patients have a predisposition to cancer, in particular osteosarcoma. B |
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CID11:ID_1650688177
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dki-india-ID_1650688177
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Concluído
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15 August 2026
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