Schizophrenia with the 22q11.2 deletion and additional genetic defects: Case history

British Journal of Psychiatry

Volumn 199, Issue 3, 2011, Pages 245-246

  Toyosima, M ^a   Maekawa, Motoko ^a   Toyota, T ^a   Iwayama, Y ^a   Arai, M ^b   Ichikawa, T ^b   Miyashita, M ^b   Arinami, T ^c   Itokawa, M ^a,b   Yoshikawa, T ^a  

^a RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^b TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^c UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

PENTOSIDINE; QUETIAPINE; RISPERIDONE;

ADULT; ARTICLE; AUDITORY HALLUCINATION; CASE REPORT; CHROMOSOME DELETION 22Q11; DIVERGENT STRABISMUS; ECHOCARDIOGRAPHY; EVALUATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FRAMESHIFT MUTATION; GENETIC DISORDER; HOSPITAL ADMISSION; HUMAN; HYPOCALCEMIA; INTELLIGENCE QUOTIENT; POLYMERASE CHAIN REACTION; RISK FACTOR; SCHIZOPHRENIA; STRABISMUS;

ADULT; ARGININE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; EXOTROPIA; FEMALE; FRAMESHIFT MUTATION; GENETIC PREDISPOSITION TO DISEASE; HOMEODOMAIN PROTEINS; HUMANS; LACTOYLGLUTATHIONE LYASE; LYSINE; POLYMERASE CHAIN REACTION; SCHIZOPHRENIA; TRANSCRIPTION FACTORS;

EID: 80052396769     PISSN: 00071250     EISSN: 14721465     Source Type: Journal    
DOI: 10.1192/bjp.bp.111.093849     Document Type: Article

References (7)

1. Karayiorgou M., Simon T.J., Gogos J.A. 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia. Nat Rev Neurosci 2010; 11: 402-416
2. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders (3rd edn, revised) (DSM-III-R). APA, 1987.
3. Arinami T., Ohtsuki T., Takase K., Shimizu H., Yoshikawa T., Horigome H., et al. Screening for 22q11 deletions in a schizophrenia population. Schizophr Res 2001; 52: 167-170 (Pubitemid 33052507)
4. Arai M., Yuzawa H., Nohara I., Ohnishi T., Obata N., Iwayama Y., et al. Enhanced carbonyl stress in a subpopulation of schizophrenia. Arch Gen Psychiatry 2010; 67: 589-597
5. Toyota T., Yoshitsugu K., Ebihara M., Yamada K., Ohba H., Fukasawa M., et al. Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B. Hum Mol Genet 2004; 13: 551-561 (Pubitemid 38313214)
6. Vassos E., Collier D.A., Holden S., Patch C., Rujescu D., St Clair D., et al. Penetrance for copy number variants associated with schizophrenia. Hum Mol Genet 2010; 19: 3477-3481
7. Thornalley P.J. The glyoxalase system in health and disease. Mol Aspects Med 1993; 14: 287-371.