Baller-Gerold syndrome (Q93984)

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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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ID_1650688177
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    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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