Association between complete corpus callosum agenesis and recent-onset schizophrenia: A case report

• Published in: European psychiatry Vol. 64; no. S1; p. S244
• Main Authors: Abassi, B., Fekih-Romdhane, F., Maktouf, H., Cheour, M.
• Format: Journal Article
• Language: English
• Published: Paris Cambridge University Press 01-04-2021
• Subjects: Abstract; Association; Case reports; corpus callosum agenesis; E-Poster Presentation; recent-onset schizophrenia; Schizophrenia
• ISSN: 0924-9338; 1778-3585
• DOI: 10.1192/j.eurpsy.2021.655

IntroductionCorpus callosum agenesis (CCA) is a rare congenital disorder in which there is a partial or complete absence of the corpus callosum. Within the framework of an anatomoclinical approach to schizophrenia, a few studies have focused on its association with neurological disorders, including CCA.ObjectivesIn this perspective, we report a rare case of an adolescent with intellectual disability, with whose complete CCA was revealed by a recent-onset schizophrenia.MethodsA case report and literature review.ResultsThe teenager M.A. is from a first degree consanguineous marriage. He had no family history, no special habits and no history of seizures. Since early childhood, he had had a psychomotor acquisition delay and relationship difficulties that tended to worsen later. At school, he was teased by his peers and failed 4 times in different rows. At the age of 15, he dropped out of school. Verbal and physical aggressiveness, soliloquy, unmotivated laughter and vague ideas of persecution suddenly appeared, hence his psychiatric consultation one month later. Neuropsychological tests indicated current low Intelligence Quotient (60). Brain imaging revealed complete ACC (see Figure 1). He was diagnosed with schizophrenia and put on antipsychotic treatment at adequate doses and durations, with poor therapeutic response.ConclusionsOur observation provides additional support for neurodevelopmental models of schizophrenia, and confirms literature data indicating that severe structural brain abnormalities would lead to early onset psychotic symptoms which are often refractory to pharmacological treatments