Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome. Issue 3 (28th July 2022)

• Record Type: Journal Article
• Authors: Nagai, Yasuhito; Nishioka, Masaki; Tanaka, Tatsuki; Shimano, Takahisa; Kirino, Eiji; Suzuki, Toshihito; Kato, Tadafumi
• Is Part Of: PCN reports. Volume 1:Issue 3(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-07-28
• Subjects: 22q11.2 deletion syndrome -- autism spectrum disorder -- HERC1 -- Rubinstein–Taybi syndrome -- schizophrenia; Psychiatry; Neurosciences; Periodicals; 616.89
• DOI: 10.1002/pcn5.34
• Languages: English
• ISSNs: 1323-1316

Abstract

Abstract: Background: Rubinstein–Taybi syndrome (RTS) is a rare autosomal‐dominant disease. Almost all cases are sporadic and attributed to de novo variant. Psychotic symptoms in RTS are rare and have been reported in only a few published cases. On the other hand, 22q11.2 deletion syndrome is the most common chromosomal microdeletion in humans. The 22q11.2 deletion is well recognized as a risk factor for schizophrenia. Here, we present a schizophrenic psychosis case clinically diagnosed as RTS but resolved as carrying 22q11.2 deletion by genomic analysis. Case presentation: A 38‐year‐old Japanese male was admitted to our hospital due to psychotic symptoms. He had been diagnosed with RTS based on physical characteristics at the age of 9 months. On admission, we performed whole exome sequencing. He had no pathogenic variant in CREBBP or EP300 . We detected 2.5 Mb deletion on 22q11.2 and one rare loss‐of‐function variant in a loss‐of‐function‐constrained gene ( MTSS1 ) and three rare missense variants in missense‐constrained genes ( CELSR3, HERC1, and TLN1 ). Psychotic symptoms were ameliorated by the treatment of risperidone. Conclusion: The psychiatric manifestation and genomic analysis may be a clue to detecting 22q11.2 deletion syndrome in undiagnosed patients. The reason for similarity in physical characteristics in 22q11.2 deletion syndrome and RTS remains unresolved. The 22q11.2 deletion and HERC1 contribute to the patient's phenotype. Abstract : Venn diagram for explanation of the overlap phenotypes.