Baller‐Gerold syndrome: An 11th case of craniosynostosis and radial aplasia

1 December 1990

journal article
research article
Published by Wiley in American Journal of Medical Genetics

Vol. 37 (4) , 447-450
https://doi.org/10.1002/ajmg.1320370403

Abstract

We report on a patient with craniosynostosis, left radius aplasia, right radius hypoplasia, and other congenital anomalies. This is the 11th reported case of the Baller‐Gerold syndrome. Autosomal recessive inheritance of this syndrome is suggested by evidence of probable parental consanguinity.

Keywords

This publication has 6 references indexed in Scilit:

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