Challman Thomas D, Barbaresi William J, Katusic Slavica K, Weaver Amy
Department of Pediatric and Adolescent Medicine, Division of Developmental and Behavioral Pediatrics, Mayo Clinic, 200 First Street SW, Rochester, Minnesota, USA.
J Autism Dev Disord. 2003 Apr;33(2):187-92. doi: 10.1023/a:1022995611730.
Little information is available regarding the yield of the medical evaluation of children diagnosed with pervasive developmental disorder-not otherwise specified (PDD-NOS) compared to children diagnosed with autistic disorder. Medical records were reviewed for 182 patients less than 18 years of age with either PDD-NOS or autistic disorder evaluated between 1994 and 1998 at Mayo Clinic. A condition likely to be etiologically relevant was identified in 6/117 (5.1%) patients diagnosed with PDD-NOS and 2/65 (3.1%) patients diagnosed with autistic disorder. Genetic disorders, both chromosomal and single-gene, were the most commonly identified conditions. Seizure disorders, electroencephalogram abnormalities, and anomalies on brain imaging were common in both groups. The likelihood of uncovering an etiologically relevant condition in children diagnosed with either PDD-NOS or autistic disorder may be equivalent. The scope of the etiological search in an individual patient with an autistic spectrum disorder should not be limited by the specific diagnostic category.
与被诊断为孤独症谱系障碍的儿童相比,关于被诊断为广泛性发育障碍(未另作说明,PDD-NOS)的儿童医学评估结果的信息较少。回顾了梅奥诊所1994年至1998年间评估的182例年龄小于18岁、患有PDD-NOS或孤独症谱系障碍的患者的病历。在被诊断为PDD-NOS的117例患者中有6例(5.1%)以及被诊断为孤独症谱系障碍的65例患者中有2例(3.1%)发现了可能与病因相关的情况。染色体和单基因的遗传性疾病是最常发现的情况。癫痫症、脑电图异常以及脑成像异常在两组中都很常见。在被诊断为PDD-NOS或孤独症谱系障碍的儿童中发现与病因相关情况的可能性可能相当。对患有孤独症谱系障碍的个体患者进行病因排查的范围不应受特定诊断类别的限制。