Baller–Gerold syndrome
SYNOSTOSIS CHARACTERIZED BY CORONAL CRANIOSYNOSTOSIS, SHORT STATURE, AND APLASIA OR HYPOPLASIA OF THE RADIAL BONE
Baller-Gerold syndrome
Baller–Gerold syndrome (BGS) is a rare genetic syndrome that involves premature fusion of the skull bones and malformations of facial, forearm and hand bones. The symptoms of Baller–Gerold syndrome overlap with features of a few other genetics disorders: Rothmund–Thomson syndrome and RAPADILINO syndrome.