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).

Absent radius

Missing radius bone associated with congenital failure of development.


Total: 2

                       


(per page)
PMID (PMCID)
9733037
 MALE
Baller-Gerold syndrome associated with congenital portal venous malformation.
Savarirayan R, Tomlinson P, Thompson E.
J Med Genet. 1998;35(9):767-9.
We report a 4 year old boy in whom the clinical features of craniosynostosis and bilateral absent radii led to a diagnosis of Baller-Gerold syndrome.
9786296
 MALE Infant, Newborn
Immunodeficiency in a patient with Baller-Gerold syndrome: a reason for early demise?
Golombek SG, Clement LT, Begleiter M, Truog WE.
South Med J. 1998;91(10):966-9.
We describe the case of a 37-week-old, small-for-gestational-age, white baby girl born with Baller-Gerold syndrome (BGS), with craniosynostosis and partial absence of the corpus callosum, absent radius, and syndactyly.