The velocardiofacial syndrome in psychiatry

被引:13
作者
Feinstein, C [1 ]
Eliez, S [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Div Child & Adolescent Psychiat, Stanford, CA 95305 USA
关键词
D O I
10.1097/00001504-200009000-00004
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Velocardiofacial syndrome (VCFS) is a genetic disability syndrome that is caused, in most cases, by a de-novo 3 Mb microdeletion at chromosome region 22q11.2. The behavioral phenotype includes characteristic developmental, cognitive, and linguistic deficits, and psychiatric disorders, including childhood abnormalities of attention, mood, and anxiety. Recently, it was established that approximately 30% of people with VCFS develop schizophrenia, establishing VCFS as the first known genetic cause of schizophrenia. There has been recent progress in describing the molecular biology of the deletion site, characterizing the behavioral phenotype, and in defining the structural brain abnormalities in VCFS. However, numerous knowledge gaps remain in tracing the pathways from gene expression to brain structure, and to cognitive and psychiatric symptoms. Curr Opin Psychiatry 13:485-490; (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:485 / 490
页数:6
相关论文
共 68 条
[41]  
McDonald-McGinn DM, 1999, GENET COUNSEL, V10, P11
[42]   BRAIN ANOMALIES IN VELO-CARDIO-FACIAL SYNDROME [J].
MITNICK, RJ ;
BELLO, JA ;
SHPRINTZEN, RJ .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 54 (02) :100-106
[43]   Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern [J].
Moss, EM ;
Batshaw, ML ;
Solot, CB ;
Gerdes, M ;
McDonald-McGinn, DM ;
Driscoll, DA ;
Emanuel, BS ;
Zackai, EH ;
Wang, PP .
JOURNAL OF PEDIATRICS, 1999, 134 (02) :193-198
[44]   Chromosome 22q11 deletions - An under-recognised cause of idiopathic learning disability [J].
Murphy, KC ;
Jones, RG ;
Griffiths, E ;
Thompson, PW ;
Owen, MJ .
BRITISH JOURNAL OF PSYCHIATRY, 1998, 172 :180-183
[45]   High rates of schizophrenia in adults with velo-cardio-facial syndrome [J].
Murphy, KC ;
Jones, LA ;
Owen, MJ .
ARCHIVES OF GENERAL PSYCHIATRY, 1999, 56 (10) :940-945
[46]   Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles [J].
Palmatier, MA ;
Kang, AM ;
Kidd, KK .
BIOLOGICAL PSYCHIATRY, 1999, 46 (04) :557-567
[47]  
Papolos DF, 1996, AM J PSYCHIAT, V153, P1541
[48]   Ultra-ultra rapid cycling bipolar disorder is associated with the low activity catecholamine-O-methyltransferase allele [J].
Papolos, DF ;
Veit, S ;
Faedda, GL ;
Saito, T ;
Lachman, HM .
MOLECULAR PSYCHIATRY, 1998, 3 (04) :346-349
[49]   PSYCHOTIC ILLNESS IN PATIENTS DIAGNOSED WITH VELO-CARDIO-FACIAL SYNDROME AND THEIR RELATIVES [J].
PULVER, AE ;
NESTADT, G ;
GOLDBERG, R ;
SHPRINTZEN, RJ ;
LAMACZ, M ;
WOLYNIEC, PS ;
MORROW, B ;
KARAYIORGOU, M ;
ANTONARAKIS, SE ;
HOUSMAN, D ;
KUCHERLAPATI, R .
JOURNAL OF NERVOUS AND MENTAL DISEASE, 1994, 182 (08) :476-478
[50]   Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome [J].
Roberts, C ;
Daw, SCM ;
Halford, S ;
Scambler, PJ .
HUMAN MOLECULAR GENETICS, 1997, 6 (02) :237-245