Baller-Gerold syndrome (Q93984): Difference between revisions

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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
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