BEHAVIOR PROBLEMS IN ANGELMAN SYNDROME

被引:95
作者
SUMMERS, JA
ALLISON, DB
LYNCH, PS
SANDLER, L
机构
[1] KENNEDY KRIEGER INST,BALTIMORE,MD
[2] JOHNS HOPKINS UNIV,SCH MED,BALTIMORE,MD
[3] ST LUKES ROOSEVELT HOSP,NEW YORK,NY
[4] COLUMBIA UNIV,COLL PHYS & SURG,NEW YORK,NY
关键词
D O I
10.1111/j.1365-2788.1995.tb00477.x
中图分类号
G76 [特殊教育];
学科分类号
040109 ;
摘要
Angelman syndrome (AS) is a genetic disorder that is associated with a deletion on chromosome Ig, and is characterized by abnormalities or impairments in neurological, motor and intellectual functioning. While behaviour problems have been reported in clients with AS, relatively little is known about their developmental course and outcome. In this study, data on the nature and prevalence of behaviour problems among clients with AS were gathered from two sources: (I) a review of published case reports; and (2) parent responses to a survey of behaviour problems in a small (n=II) sample of children with AS. Data from both sources showed that behaviour problems were present in males and females of all ages, and included language deficits, excessive laughter, hyperactivity, short attention span, problems with eating and sleeping, aggression, noncompliance, mouthing of objects, tantrums, and repetitive and stereotyped behaviour. Identification and treatment of severe behaviour problems in clients with AS may improve their adaptive functioning.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 48 条
[1]  
ACHENBACH TM, 1983, MANUAL CHILD BEHAVIO
[2]  
ANGELMAN H, 1965, DEV MED CHILD NEUROL, V7, P681
[3]  
BARAITSER M, 1987, CLIN GENET, V31, P323
[4]  
BERG J M, 1990, International Review of Psychiatry, V2, P53, DOI 10.3109/09540269009028271
[5]  
BERG JM, 1975, AM J DIS CHILD, V123, P72
[6]   HAPPY PUPPET SYNDROME [J].
BOWER, BD ;
JEAVONS, PM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1967, 42 (223) :298-&
[7]   THE EEG IN EARLY DIAGNOSIS OF THE ANGELMAN (HAPPY PUPPET) SYNDROME [J].
BOYD, SG ;
HARDEN, A ;
PATTON, MA .
EUROPEAN JOURNAL OF PEDIATRICS, 1988, 147 (05) :508-513
[8]  
BROMLEY BE, 1991, MENT RETARD, V29, P275
[9]   CLINICAL RESEARCH ON ANGELMAN SYNDROME IN THE UNITED-KINGDOM - OBSERVATIONS ON 82 AFFECTED INDIVIDUALS [J].
CLAYTONSMITH, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 46 (01) :12-15
[10]   DETECTION OF A 15Q DELETION IN A CHILD WITH ANGELMAN SYNDROME BY CYTOGENETIC ANALYSIS AND FLOW-CYTOMETRY [J].
COOKE, A ;
TOLMIE, JL ;
GLENCROSS, FJ ;
BOYD, E ;
CLARKE, MM ;
DAY, R ;
STEPHENSON, JBP ;
CONNOR, JM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (04) :545-549