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Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate
Baller Gerold Syndrome (BGS) is a rare autosomal recessive disorder that is apparent at birth. The disorder is characterized by distinctive malformations of the skull and facial area and bones of the forearms and hands. We are reporting a new case of BGS in a 10-month-old female child born of an epi...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781148/ https://www.ncbi.nlm.nih.gov/pubmed/19966981 http://dx.doi.org/10.4103/0972-2327.40228 |