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Hippocampal Malrotation is Associated with Chromosome 22q11.2 Microdeletion
BACKGROUND: Patients with chromosome 22q11.2 deletion syndrome (22q11DS) are at a seven fold increased risk of developing seizures. However, only a fraction of these patients exhibit structural abnormalities such as polymicrogyria (PMG) and periventricular nodular heterotopia (PNH) that are known to...
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| Publicado no: | Can J Neurol Sci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4459860/ https://ncbi.nlm.nih.gov/pubmed/23968937 |
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