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Baller-Gerold syndrome associated with congenital portal venous malformation.

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. Additional congenital abnormalities included midface hypoplasia, atrial and ventricular septal defects, right hydronephrosis, partial sacral agenesis,...

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Detalhes bibliográficos
Main Authors: Savarirayan, R, Tomlinson, P, Thompson, E
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051431/
https://ncbi.nlm.nih.gov/pubmed/9733037
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