A practical diagnostic approach to mental deficiency in 2002

被引:12
作者
des Portes, V
Livet, MO
Vallée, L
机构
[1] Ctr Hosp Reg & Univ Lille, Hop Roger Salengro, Pediat Clin, Serv Neuropediat, F-59037 Lille, France
[2] Ctr Hosp Pays dAix, Serv Pediat, Aix En Provence, France
[3] Hop St Vincent de Paul, Serv Neuropediat, F-75674 Paris, France
来源
ARCHIVES DE PEDIATRIE | 2002年 / 9卷 / 07期
关键词
mental retardation; diagnostic techniques and procedures; child;
D O I
10.1016/S0929-693X(01)00973-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The identification of an etiology in children with mental deficiency is a major challenge in routine pediatrics. As the result of a workshop leaded by the Societe francaise de neurologie pediatrique (SFNP), we propose a three steps diagnostic procedure, taking into account several frequent clinical observations leading to further targeted investigations. The yield of systematic imaging and biological screening remains very low, when performed for a non specific isolated mental retardation, without any characteristic clinical features. Yet, it is mandatory for an accurate genetic counseling to know not only the clinical diagnosis of developmental delay, but also the pathophysiology and the underlying molecular mechanism. The SFNPs proposal points out the necessity of a comprehensive clinical process including cautious neurodevelopmental assessment, reliable cognitive and adaptive skills evaluation, and collaboration between different specialists. (C) 2002 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:709 / 725
页数:17
相关论文
共 27 条
  • [1] [Anonymous], 1994, Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV), V4th
  • [2] A COMMUNITY STUDY OF SEVERE MENTAL-RETARDATION IN THE WEST MIDLANDS AND THE IMPORTANCE OF THE FRAGILE X-CHROMOSOME IN ITS ETIOLOGY
    BUNDEY, S
    WEBB, TP
    THAKE, A
    TODD, J
    [J]. JOURNAL OF MEDICAL GENETICS, 1985, 22 (04) : 258 - 266
  • [3] Aetiological findings and associated factors in children with severe mental retardation
    Cans, C
    Wilhelm, L
    Baille, MF
    du Mazaubrun, C
    Grandjean, H
    Rumeau-Rouquette, C
    [J]. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 1999, 41 (04) : 233 - 239
  • [4] Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
    de Vries, BBA
    White, SM
    Knight, SJL
    Regan, R
    Homfray, T
    Young, ID
    Super, M
    McKeown, C
    Splitt, M
    Quarrell, OWJ
    Trainer, AH
    Niermeijer, MF
    Malcolm, S
    Flint, J
    Hurst, JA
    Winter, RM
    [J]. JOURNAL OF MEDICAL GENETICS, 2001, 38 (03) : 145 - 150
  • [5] doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
    des Portes, V
    Francis, F
    Pinard, JM
    Desguerre, I
    Moutard, ML
    Snoeck, I
    Meiners, LC
    Capron, F
    Cusmai, R
    Ricci, S
    Motte, J
    Echenne, B
    Ponsot, G
    Dulac, O
    Chelly, J
    Beldjord, C
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (07) : 1063 - 1070
  • [6] Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey
    deVries, BBA
    vandenOuweland, AMW
    Mohkamsing, S
    Duivenvoorden, HJ
    Mol, E
    Gelsema, K
    vanRijn, M
    Halley, DJJ
    Sandkuijl, LA
    Oostra, BA
    Tibben, A
    Niermeijer, MF
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (03) : 660 - 667
  • [7] Fernell E, 1998, DEV MED CHILD NEUROL, V40, P608
  • [8] X-LINKED MENTAL-RETARDATION
    GLASS, IA
    [J]. JOURNAL OF MEDICAL GENETICS, 1991, 28 (06) : 361 - 371
  • [9] GRAHAM SM, 1993, J PAEDIAT CLIN HLTH, V5, P360
  • [10] EPIDEMIOLOGY OF MENTAL-RETARDATION - A SWEDISH SURVEY
    HAGBERG, B
    KYLLERMAN, M
    [J]. BRAIN & DEVELOPMENT, 1983, 5 (05) : 441 - 449