Preferred Label : Baller-Gerold syndrome;
ICD-11 definition : Baller-Gerold syndrome is an autosomal recessive disorder characterized 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;
Origin ID : 1650688177;
Automatic exact mappings (from CISMeF team)
Baller-Gerold syndrome is an autosomal recessive disorder characterized 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
