Lithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports

BACKGROUND: Phelan-Mc Dermid syndrome is a contiguous disorder resulting from 22q13.3 deletion implicating the SHANK3 gene. The typical phenotype includes neonatal hypotonia, moderate to severe intellectual disability, absent or delayed speech, minor dysmorphic features and autism or autistic-like b...

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Detalles Bibliográficos
Autores principales: Serret, Sylvie, Thümmler, Susanne, Dor, Emmanuelle, Vesperini, Stephanie, Santos, Andreia, Askenazy, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428105/
https://www.ncbi.nlm.nih.gov/pubmed/25947967
http://dx.doi.org/10.1186/s12888-015-0490-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428105/
https://www.ncbi.nlm.nih.gov/pubmed/25947967
http://dx.doi.org/10.1186/s12888-015-0490-1

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