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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Bibliographic Details
Main Author: Rocha, J (author)
Other Authors: Guerra, C (author), Oliveira, R (author), Dória, S (author), Rego, R (author), Rosas, MJ (author)
Format: article
Language:eng
Published: 2013
Subjects:
Duplicação Cromossómica
Cromossoma Humano Par 15
Deficiência Intelectual
Espasmos Infantis
Online Access:http://hdl.handle.net/10400.23/545
Country:Portugal
Oai:oai:repositorio.hospitaldebraga.pt:10400.23/545

Internet

http://hdl.handle.net/10400.23/545

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