Catalog

Baller-Gerold syndrome

No MMS code

Link to WHO Definition

Baller-Gerold syndrome – http://id.who.int/icd/entity/1650688177

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

Parents