Social and emotional problems in children with neurofibromatosis type 1: Evidence and proposed interventions

被引:88
作者
Johnson, NS [1 ]
Saal, HM [1 ]
Lovell, AM [1 ]
Schorry, EK [1 ]
机构
[1] Childrens Hosp, Ctr Med, Div Human Genet, Cincinnati, OH 45229 USA
关键词
D O I
10.1016/S0022-3476(99)70296-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: To describe social and emotional problems in children and adolescents with neurofibromatosis type I (NF1) and propose interventions. Our hypothesis is that children with NF1 will have significantly more social and emotional problems, compared with their unaffected siblings and children in the general population. Study design: Ferry-three children with NF1 and 22 unaffected siblings (ages 5 to 18 years) were assessed with a standardized test completed by parents and teachers (the Child Behavior Checklist). Results: As with other aspects of NF1, there was variable expressivity. However, when rated by parents, children with NF1 had significantly more problems in comparison with test norms or unaffected siblings on 7 of 8 scales: Social Problems, Attention Problems, Anxiety/Depression, Withdrawal, Thought Problems, Somatic Complaints, and Aggressive Behavior. Children with NF1 also scored lower than unaffected siblings on measures assessing sports and other activities. Teachers reported fewer differences. Conclusions: We propose interventions in the form of information for parents; early screening and treatment for speech, motor, and cognitive problems; and an increased level of intervention to prevent and treat psychologic problems, including systematic screening with standardized tests.
引用
收藏
页码:767 / 772
页数:6
相关论文
共 25 条
[1]  
ABLON J, 1992, PSYCHOSOCIAL ASPECTS, P49
[2]  
ACHENBACH TM, 1991, MANUAL CHILD BEHAV C, P191
[3]   Growth rate characteristics of acoustic neuromas associated with neurofibromatosis type 2 [J].
Abaza, MM ;
Makariou, E ;
Armstrong, M ;
Lalwani, AK .
LARYNGOSCOPE, 1996, 106 (06) :694-699
[4]   NEUROFIBROMATOSIS TYPE-1 (NF1) - KNOWLEDGE, EXPERIENCE, AND REPRODUCTIVE DECISIONS OF AFFECTED PATIENTS AND FAMILIES [J].
BENJAMIN, CM ;
COLLEY, A ;
DONNAI, D ;
KINGSTON, H ;
HARRIS, R ;
KERZINSTORRAR, L .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (07) :567-574
[5]  
COLEMAN SL, 1987, THESIS U HOUSTON HOU
[6]  
Dilts CV, 1996, J DEV BEHAV PEDIATR, V17, P229
[7]   NEUROFIBROMATOSIS TYPE-1 (RECKLINGHAUSENS DISEASE) - NEUROLOGIC AND COGNITIVE ASSESSMENT WITH SIBLING CONTROLS [J].
ELDRIDGE, R ;
DENCKLA, MB ;
BIEN, E ;
MYERS, S ;
KAISERKUPFER, MI ;
PIKUS, A ;
SCHLESINGER, SL ;
PARRY, DM ;
DAMBROSIA, JM ;
ZASLOFF, MA ;
MULVIHILL, JJ .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1989, 143 (07) :833-837
[8]   NEUROFIBROMATOSIS TYPE-1 - THE COGNITIVE PHENOTYPE [J].
HOFMAN, KJ ;
HARRIS, EL ;
BRYAN, RN ;
DENCKLA, MB .
JOURNAL OF PEDIATRICS, 1994, 124 (04) :S1-S8
[9]  
Huson S. M., 1994, P355
[10]  
KAMPHAUS RW, 1996, CLIN ASSESSMENT CHIL, P127