Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion

被引：40

作者：

Vucurovic, Ksenija ^{[1
]}

Landais, Emilie ^{[2
]}

Delahaigue, Cecile ^{[1
]}

Eutrope, Julien ^{[1
]}

Schneider, Anouck ^{[2
,3
]}

Leroy, Camille ^{[2
]}

Kabbaj, Hamza ^{[1
]}

Motte, Jacques ^{[4
]}

Gaillard, Dominique ^{[2
]}

Rolland, Anne-Catherine ^{[1
]}

Doco-Fenzy, Martine ^{[2
,5
]}

机构：

[1] Univ Hosp Reims, Dept Child & Adolescent Psychiat, Reims, France

[2] Univ Hosp Reims, Dept Genet, Biol Sect, Reims, France

[3] CHU Montpellier, Dept Genet, Montpellier, France

[4] SFR CAP SANTE REIMS, CHU REIMS, Amer Mem Hosp, Dept Pediat, Reims, France

[5] SFR CAP SANTE REIMS, EA 3801, Reims, France

来源：

EUROPEAN JOURNAL OF MEDICAL GENETICS | 2012年 / 55卷 / 11期

关键词：

SHANK3; deletion; Bipolar affective disorder; 22q13 deletion syndrome; Dementia onset; Dementia of Alzheimer's type; EXPRESSION; PROTEIN; SLEEP;

D O I：

10.1016/j.ejmg.2012.07.009

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

The SHANK3 protein is a scaffold protein known to stabilize metabotropic glutamate receptor mGluR5 in the post-synaptic membrane of neurons. It is associated with genetic vulnerability in autism and schizophrenia. Here we report the case of an 18 year-old male patient who displayed psychiatric features of bipolar affective disorder associated with early setting of dementia. This mental status is related to sporadic occurrence of SHANK3 gene complex multiple deletions. A low beta amyloid protein rate (479 mg/L) found in cerebrospinal fluid suggests a possible link between SHANK3 deletion syndrome-associated regression and dementia of Alzheimers's type. In addition, we propose an overview of the phenotype related to SHANK3 deletion. (C) 2012 Elsevier Masson SAS. All rights reserved.

引用

页码：625 / 629

页数：5

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