Two children with muscular dystrophies ascertained due to referral for diagnosis of autism

被引:21
作者
Zwaigenbaum, L
Tarnopolsky, M
机构
[1] McMaster Univ, Dept Pediat, Hamilton, ON, Canada
[2] McMaster Univ, Dept Med Neurol & Rehabil, Hamilton, ON, Canada
关键词
autism; pervasive developmental disorder; muscular dystrophy; hypotonia;
D O I
10.1023/A:1022947728569
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
We report two children who were referred for diagnostic assessment for autism and were subsequently determined to have a muscular dystrophy (MD). Each child had a history of speech delay and social impairments, but also had motor delays that had not previously been investigated. Both children met diagnostic criteria for autism spectrum disorders on standardized assessment. Each child was hypotonic and had other mild motor impairments. Serum creatine kinase (CK) activity was markedly elevated in each child, and subsequent muscle biopsy led to diagnosis of Becker's MD and congenital (autosomal recessive) MD, respectively. These cases highlight the importance of a thorough neuromotor examination for all children with suspected autism spectrum disorders.
引用
收藏
页码:193 / 199
页数:7
相关论文
共 43 条
  • [21] The Autism Diagnostic Observation Schedule-Generic: A standard measure of social and communication deficits associated with the spectrum of autism
    Lord, C
    Risi, S
    Lambrecht, L
    Cook, EH
    Leventhal, BL
    DiLavore, PC
    Pickles, A
    Rutter, M
    [J]. JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2000, 30 (03) : 205 - 223
  • [22] AUTISM DIAGNOSTIC INTERVIEW-REVISED - A REVISED VERSION OF A DIAGNOSTIC INTERVIEW FOR CAREGIVERS OF INDIVIDUALS WITH POSSIBLE PERVASIVE DEVELOPMENTAL DISORDERS
    LORD, C
    RUTTER, M
    LECOUTEUR, A
    [J]. JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1994, 24 (05) : 659 - 685
  • [23] Correlations between individual clinical manifestations and CTG repeat amplification in myotonic dystrophy
    Marchini, C
    Lonigro, R
    Verriello, L
    Pellizzari, L
    Bergonzi, P
    Damante, G
    [J]. CLINICAL GENETICS, 2000, 57 (01) : 74 - 82
  • [24] Brain dystrophin, neurogenetics and mental retardation
    Mehler, MF
    [J]. BRAIN RESEARCH REVIEWS, 2000, 32 (01) : 277 - 307
  • [25] Molecular characterisation of Duchenne muscular dystrophy and phenotypic correlation
    Mital, A
    Kumari, D
    Gupta, M
    Goyle, S
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 157 (02) : 179 - 186
  • [26] BECKER MUSCULAR-DYSTROPHY - CORRELATION OF DELETION TYPE WITH CLINICAL SEVERITY
    NORMAN, AM
    THOMAS, NST
    KINGSTON, HM
    HARPER, PS
    [J]. JOURNAL OF MEDICAL GENETICS, 1990, 27 (04) : 236 - 239
  • [27] Paul M, 1997, DEV MED CHILD NEUROL, V39, P280
  • [28] PEGORARO E, 1994, AM J HUM GENET, V54, P989
  • [29] Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients
    Perini, GI
    Menegazzo, E
    Ermani, M
    Zara, M
    Gemma, A
    Ferruzza, E
    Gennarelli, M
    Angelini, C
    [J]. BIOLOGICAL PSYCHIATRY, 1999, 46 (03) : 425 - 431
  • [30] Polakoff R J, 1998, Semin Pediatr Neurol, V5, P116, DOI 10.1016/S1071-9091(98)80027-2