| Literature DB >> 29183893 |
Kevin Lally1, Nuraini Ibrahim1,2, Mary Kelly1,2, Gautam Gulati1.
Abstract
A 21-year-old woman with moderate learning disability secondary to chromosome 2 microdeletion at q37 was admitted to a general adult psychiatric ward following a period of agitation with incessant pressure of speech, nihilistic delusions and worsening of sleep and eating patterns. Her presentation was preceded for a number of weeks by social stressors of an ill family member and another family member moving away. She had also been diagnosed and treated for a respiratory infection several weeks prior to presentation. Her presentation improved with low-dose antipsychotic medication and parallel input from the general adult mental health team and the psychiatry of intellectual disability team. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: congenital disorders; genetics; psychotic disorders (incl schizophrenia); therapeutic indications
Mesh:
Year: 2017 PMID: 29183893 PMCID: PMC5720329 DOI: 10.1136/bcr-2017-221012
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X