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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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| Publicat a: | Can J Neurol Sci |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4459860/ https://ncbi.nlm.nih.gov/pubmed/23968937 |
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