The authors declare that they have no competing interests.
Both authors were equally involved in the collection of data and in drafting the manuscript. Both authors read and approved the final manuscript.
Mental comorbidities, such as phobia, obsessive compulsive symptoms and anxiety disorders, are common in Williams syndrome. However, psychotic symptoms are rare in these patients. We report a case of psychosis in a patient with Williams syndrome.
A 23-year-old Caucasian woman with Williams syndrome arrived at the emergency room with persecutory delusions, auditory and verbal hallucinations, soliloquies and psychomotor agitation. These symptoms were consistently present for 2 months. No evidence of other medical illnesses or psychoactive substances was found. There was no evidence of prior psychiatric symptoms or family history of psychiatric or neurological disorders. She was treated with antipsychotics and her symptoms were resolved.
We describe a rare case of a patient with Williams syndrome who experienced a nonorganic psychotic episode. Literature on this topic is scarce and, therefore, this case report intends to add further data about this comorbidity.
Huang L, Sadler L, O’Riordan MA, Robin NH: Delay in diagnosis of Williams syndrome. ClinPediatr (Phila). 2002, 41: 257-261. 10.1177/000992280204100410. CrossRef
Morris CA: Williams syndrome. http://www.ncbi.nlm.nih.gov/books/NBK1249/,
Stinton C, Tomlinson K, Estes Z: Examining reports of mental health in adults with Williams syndrome. Res DevDisabil. 2012, 33: 144-152. 10.1016/j.ridd.2011.09.002. CrossRef
American Academy of Pediatrics: Health care supervision for children with Williams syndrome. Pediatrics. 2001, 107: 1192-1204. CrossRef
- Williams syndrome and psychosis: a case report
- BioMed Central