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Elevated homocysteine and N-methyl-d-aspartate-receptor antibodies as a cause of behavioural and cognitive decline in 22q11.2 deletion syndrome

A 19-year-old male with 22q11.2 deletion syndrome presented with a 4-year history of cognitive decline and symptoms suggestive of atypical psychosis. Potential for elevated homocysteine and NMDA-receptor antibodies in the pathogenesis of his symptoms was investigated. He had elevated blood homocyste...

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Detalles Bibliográficos
Autores principales: Vann Jones, Simon, Banerjee, Subimal, Smith, A David, Refsum, Helga, Lennox, Belinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751082/
https://www.ncbi.nlm.nih.gov/pubmed/29308211
http://dx.doi.org/10.1093/omcr/omx076