Baller-Gerold syndrome (Q93984): Difference between revisions
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A síndrome de Baller-Gerold é uma doença autossômica recessiva caracterizada pela associação de craniossinostose coronal com anomalias dos raios radiais (oligodactilia, aplasia ou hipoplasia do polegar, aplasia ou hipoplasia do rádio). Os pacientes têm predisposição ao câncer, em particular ao osteossarcoma. | |||
| description / en | description / en | ||
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 | |||
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 |
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| 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 |
