PSYCHOPATHOLOGY OF PATIENTS TREATED EARLY FOR PHENYLKETONURIA - RESULTS OF THE GERMAN COLLABORATIVE STUDY OF PHENYLKETONURIA

被引:36
作者
BURGARD, P
ARMBRUSTER, M
SCHMIDT, E
RUPP, A
机构
[1] FREE UNIV BERLIN,DEPT PEDIAT,BERLIN,GERMANY
[2] UNIV DUSSELDORF,DEPT PEDIAT,DUSSELDORF,GERMANY
[3] UNIV GOTTINGEN,DEPT PEDIAT,GOTTINGEN,GERMANY
[4] UNIV HAMBURG,DEPT PEDIAT,HAMBURG,GERMANY
[5] UNIV MUNICH,DEPT PEDIAT,MUNICH,GERMANY
[6] UNIV MUNSTER,DEPT PEDIAT,MUNSTER,GERMANY
[7] UNIV ULM,DEPT PEDIAT,ULM,GERMANY
关键词
D O I
10.1111/j.1651-2227.1994.tb13467.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
At the age of 13 years, 60 adolescents, suffering from phenylalaninemia due to hydroxylase deficiency, and their mothers were simultaneously investigated with a standardized psychiatric interview in order to determine the adolescents' psychiatric status. Forty symptoms related to emotional disorders, antisocial and conduct disorders, hyperkinetic syndromes, and specific symptoms like psychophysiological pains, enuresis, encopresis, ties, stereotypies, and eating disorders were examined. Severity level was rated as undisturbed, mild, moderate, and severe disturbance. Comparison with a representative sample of 191 age mates revealed a double rate of moderate disturbances for the PKU sample. There was no association between severity level and sex as well as mean phenylalanine level during the first 13 years of the patients' lives. No PKU specific diagnosis could be determined. WISC-R-IQ below 90 was associated with a threefold risk of more severe disturbance and patients with more than three adverse familial circumstances had a 50% chance of getting a psychiatric diagnosis. It is concluded that the observed disturbances result from stress associated more with the chronic condition than with the increased phenylalanine level.
引用
收藏
页码:108 / 110
页数:3
相关论文
共 10 条
  • [1] COWIE VA, 1971, PHENYLKETONURIA SOME, P29
  • [2] EPIDEMIOLOGY AND COURSE OF PSYCHIATRIC-DISORDERS IN SCHOOL-AGE-CHILDREN - RESULTS OF A LONGITUDINAL-STUDY
    ESSER, G
    SCHMIDT, MH
    WOERNER, W
    [J]. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES, 1990, 31 (02): : 243 - 263
  • [3] ESSER G, 1989, MANNHEIMER ELTERN IN
  • [4] The separation of phenylpyruvic acid in urine as a metabolism anomaly in connection with imbecillitate.
    Folling, A
    [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1934, 227 : 169 - 176
  • [5] EFFECTS OF DIET AND BEHAVIOR-THERAPY ON SOCIAL AND MOTOR BEHAVIOR OF RETARDED PHENYLKETONURIC ADULTS - EXPERIMENTAL-ANALYSIS
    MARHOLIN, D
    POHL, RE
    STEWART, RM
    TOUCHETTE, PE
    TOWNSEND, NM
    KOLODNY, EH
    [J]. PEDIATRIC RESEARCH, 1978, 12 (03) : 179 - 187
  • [6] MATHEWS WS, 1986, AM J MENT DEFIC, V91, P92
  • [7] REALMUTO GM, 1986, J NERV MENT DIS, V174, P536
  • [8] BEHAVIOR DISTURBANCE IN 8-YEAR-OLD CHILDREN WITH EARLY TREATED PHENYLKETONURIA
    SMITH, I
    BEASLEY, MG
    WOLFF, OH
    ADES, AE
    [J]. JOURNAL OF PEDIATRICS, 1988, 112 (03) : 403 - 408
  • [9] AGORAPHOBIA IN PHENYLKETONURIA
    WAISBREN, SE
    LEVY, HL
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1991, 14 (05) : 755 - 764
  • [10] PSYCHOLOGICAL AND SOCIAL FINDINGS IN ADOLESCENTS WITH PHENYLKETONURIA
    WEGLAGE, J
    FUNDERS, B
    WILKEN, B
    SCHUBERT, D
    SCHMIDT, E
    BURGARD, P
    ULLRICH, K
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (07) : 522 - 525