Late-onset Lennox-Gastaut syndrome as a phenotype of 15q11.1q13.3 duplication
The clinical symptoms associated with chromosome 15q duplication syndrome manifest through a heterogeneous group of symptoms characterised by hypotonia, delay in motor skills and language development, cognitive and learning disabilities, autism spectrum disorder and refractory epilepsy. The late dev...
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| Outros Autores: | , , , , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
2013
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| Texto completo: | http://hdl.handle.net/10400.23/545 |
| País: | Portugal |
| Oai: | oai:repositorio.hospitaldebraga.pt:10400.23/545 |