Metyrosine in psychosis associated with 22q11.2 deletion syndrome: Case report

被引:11
作者
Carandang, Carlo G. [1 ]
Scholten, Monique C.
机构
[1] Dalhousie Univ, 5850-5980 Univ Ave POB 9700, Halifax, NS B3K 6R8, Canada
[2] IWK Hlth Ctr, Halifax, NS, Canada
关键词
D O I
10.1089/cap.2006.0013
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This report describes the use of metyrosine (Demser (R)) in an adolescent male with psychosis associated with the 22q11.2 deletion syndrome (velocardiofacial syndrome; VCFS), diagnosed by fluorescence in situ hybridization (FISH). He presented with multiple features of 22q11.2 deletion syndrome, including ventricular septal defect, palatal abnormalities, speech and motor delays, attention deficits, mood lability, and psychosis. After a failed trial of an atypical antipsychotic to address the psychosis, metyrosine was initiated, with significant reduction of psychotic symptoms and mood lability. Metyrosine treatment allowed this youth to live at home and to attend school, after months of recurrent psychiatric hospitalizations. The successful treatment of metyrosine for psychosis associated with VCFS represents a first in psychiatry, where a known biochemical abnormality in a psychiatric disorder was corrected by a treatment that targets the biochemical pathway, leading to reduction of psychiatric symptoms and improvement of functioning.
引用
收藏
页码:115 / 120
页数:6
相关论文
共 31 条
[1]  
ADDINGTON D, 2005, CAN J PSYCHIAT S1, V50, pS1
[2]  
ANDEN NILS-ERIK, 1967, EUR J PHARMACOL, V1, P1, DOI 10.1016/0014-2999(67)90057-X
[3]   Clinical features of 78 adults with 22q11 deletion syndrome [J].
Bassett, AS ;
Chow, EWC ;
Husted, J ;
Weksberg, R ;
Caluseriu, O ;
Webb, GD ;
Gatzoulis, MA .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 138A (04) :307-313
[4]   The schizophrenia phenotype in 22q11 deletion syndrome [J].
Bassett, AS ;
Chow, EWC ;
AbdelMalik, P ;
Gheorghiu, M ;
Husted, J ;
Weksberg, R .
AMERICAN JOURNAL OF PSYCHIATRY, 2003, 160 (09) :1580-1586
[5]   Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies [J].
Beauchesne, LM ;
Warnes, CA ;
Connolly, HM ;
Ammash, NM ;
Grogan, M ;
Jalal, SM ;
Michels, VV .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 45 (04) :595-598
[6]   Transient depressive relapse induced by catecholamine depletion - Potential phenotypic vulnerability marker? [J].
Berman, RM ;
Narasimhan, M ;
Miller, HL ;
Anand, A ;
Cappiello, A ;
Oren, DA ;
Heninger, GR ;
Charney, DS .
ARCHIVES OF GENERAL PSYCHIATRY, 1999, 56 (05) :395-403
[7]   A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population [J].
Botto, LD ;
May, K ;
Fernhoff, PM ;
Correa, A ;
Coleman, K ;
Rasmussen, SA ;
Merritt, RK ;
O'Leary, LA ;
Wong, LY ;
Elixson, EM ;
Mahle, WT ;
Campbell, RM .
PEDIATRICS, 2003, 112 (01) :101-107
[8]   Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome [J].
Gothelf, D ;
Frisch, A ;
Munitz, H ;
Rockah, R ;
Laufer, N ;
Mozes, T ;
Hermesh, H ;
Weizman, A ;
Frydman, M .
SCHIZOPHRENIA RESEARCH, 1999, 35 (02) :105-112
[9]   Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome [J].
Gothelf, D ;
Presburger, G ;
Zohar, AH ;
Burg, M ;
Nahmani, A ;
Frydman, M ;
Shohat, M ;
Inbar, D ;
Aviram-Goldring, A ;
Yeshaya, J ;
Steinberg, T ;
Finkelstein, Y ;
Frisch, A ;
Weizman, A ;
Apter, A .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 126B (01) :99-105
[10]   Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism [J].
Graf, WD ;
Unis, AS ;
Yates, CM ;
Sulzbacher, S ;
Dinulos, MB ;
Jack, RM ;
Dugaw, KA ;
Paddock, MN ;
Parson, WW .
NEUROLOGY, 2001, 57 (03) :410-416