Baller-Gerold syndrome

Baller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).

Also known as: Baller-Gerold syndrome, BALLER-Gerold syndrome, BGS, craniosynostosis with radial defects, craniosynostosis-radial aplasia syndrome

36 clinical trials for this condition and its sub-types.