Psychiatry and Clinical Psychopharmacology
Case Reports

Very Early-Onset Schizophrenia with Accompanying Obsessive-Compulsive Symptoms: A Case Report of a Female with 16p13.11 Duplication

1.

Department of Child and Adolescent Psychiatry, University of Health Sciences, Bakırköy Prof. Dr. Mazhar Osman Training and Research Hospital for Psychiatry, Neurology and Neurosurgery, İstanbul, Türkiye

2.

Department of Neurology, University of Health Sciences, Bakırköy Prof. Dr. Mazhar Osman Training and Research Hospital for Psychiatry, Neurology and Neurosurgery, İstanbul, Türkiye

3.

Division of Pediatric Genetics, Department of Pediatrics, Acibadem Mehmet Ali Aydinlar University School of Medicine, İstanbul, Türkiye

4.

Rare Diseases and Orphan Drugs Application and Research Center-ACUCARE, Acibadem Mehmet Ali Aydinlar University School of Medicine, İstanbul, Türkiye

5.

Division of Pediatric Metabolism, Department of Pediatrics, University of Health Sciences, Bakırköy Dr. Sadi Konuk Training and Research Hospital, İstanbul, Türkiye

Psychiatry and Clinical Psychopharmacology 2024; 34: 356-360
DOI: 10.5152/pcp.2024.24949
Read: 87 Downloads: 36 Published: 28 November 2024

Abstract
Psychosis is a complicated neuropsychiatric disorder that involves disruptions in perception and thinking, often resulting in hallucinations and delusions. Diagnosing and treating psychosis can be challenging due to its overlap with conditions such as obsessive-compulsive disorder. Recent research has focused on identifying the genetic and biochemical markers of psychiatric disorders, which can aid in better diagnosis and treatment. Schizophrenia, a type of psychosis, has a strong genetic component, making family history crucial for diagnosis, especially in cases with early onset. Research on very early-onset schizophrenia is limited due to the variability in its definition. Copy number variations (CNV) in the 16p13.11 chromosomal region have been associated with various neurodevelopmental disorders, including intellectual disability, autism, epilepsy, attention deficit hyperactivity disorder, and schizophrenia. The link between 16p13.11 CNVs and these conditions underscores the multifaceted role of genetics in neurodevelopmental disorders. Since these disorders often share common neuronal circuits, genetic variations affecting one disorder can impact others. Patients with atypical manifestations of psychosis and additional conditions should have a comprehensive evaluation, including further psychiatric, neuroimaging, genetic, and other specialized diagnostic tests. Taking a multidisciplinary approach is crucial for identifying all contributing factors and developing an effective treatment plan. This case report discusses a twelve-year-old female with very early-onset schizophrenia, obsessivecompulsive symptoms, intellectual disability, and a 16p13.11 duplication. It emphasizes the need for further research and a comprehensive management approach for such complex and treatment-resistant cases, which can provide valuable insights into the underlying pathophysiology of psychotic disorders.

Cite this article as: Kızıltan K, Özbezen Kızıltan E, Yerlikaya Oral E, Akgün Doğan Ö, Ersoy M, Karaçetin G. Very early-onset schizophrenia with accompanying obsessive-compulsive symptoms: A case report of a female with 16p13.11 duplication. Psychiatry Clin Psychopharmacol. 2024;34(4):356-360.

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EISSN 2475-0581