Treatment-resistant psychotic symptoms and the 15q11.2 BP1–BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature

The 15q11.2 BP1-BP2 (Burnside-Butler) deletion is a rare copy number variant impacting four genes (NIPA1, NIPA2, CYFIP1, and TUBGCP5), and carries increased risks for developmental delay, intellectual disability, and neuropsychiatric disorders (attention-deficit/hyperactivity disorder, autism, and p...

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Detalles Bibliográficos
Autores principales: Farrell, Martilias, Lichtenstein, Maya, Harner, Matthew K., Crowley, James J., Filmyer, Dawn M., Lázaro-Muñoz, Gabriel, Dietterich, Tyler E., Bruno, Lisa M., Shaughnessy, Rita A., Biondi, Tamara F., Burkholder, Stephan, Donmoyer, Jane, Berg, Jonathan S., Szatkiewicz, Jin, Sullivan, Patrick F., Josiassen, Richard C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026068/
https://www.ncbi.nlm.nih.gov/pubmed/32066678
http://dx.doi.org/10.1038/s41398-020-0725-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026068/
https://www.ncbi.nlm.nih.gov/pubmed/32066678
http://dx.doi.org/10.1038/s41398-020-0725-x

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