Smalley S L
Department of Psychiatry, University of California-Los Angeles-School of Medicine 90024, USA.
J Autism Dev Disord. 1998 Oct;28(5):407-14. doi: 10.1023/a:1026052421693.
Autism and pervasive developmental disorders (PDD) are common in tuberous sclerosis (TSC). The frequency of autism is about 25%, with 40-45% of TSC cases meeting criteria for autism or PDD. Among autistic populations, the frequency of TSC is 1-4% and perhaps as high as 8-14% among the subgroup of autistic individuals with a seizure disorder. Mental retardation (MR) and seizures, particularly infantile spasms, are significant risk factors in the development of autism/PDD in TSC; however, neither are sufficient or necessary for the development of these behaviors. The mechanism underlying the association of autism and TSC is as yet unclear but clinical features and neuroimaging investigations suggest that an abnormal TSC gene may directly influence the development of autism rather than it being a secondary effect of seizures or MR. The presence of autism/PDD may arise if the TSC gene mutations occur at critical stages of neural development in neural tissue of brain regions critical in the development of autism.
自闭症和广泛性发育障碍(PDD)在结节性硬化症(TSC)中很常见。自闭症的发生率约为25%,40 - 45%的TSC病例符合自闭症或PDD的标准。在自闭症人群中,TSC的发生率为1 - 4%,在患有癫痫症的自闭症个体亚组中可能高达8 - 14%。智力迟钝(MR)和癫痫发作,尤其是婴儿痉挛症,是TSC中自闭症/PDD发展的重要危险因素;然而,对于这些行为的发展,两者都不是充分条件或必要条件。自闭症与TSC关联的潜在机制尚不清楚,但临床特征和神经影像学研究表明,异常的TSC基因可能直接影响自闭症的发展,而不是癫痫发作或MR的继发效应。如果TSC基因突变发生在自闭症发展关键脑区神经组织的神经发育关键阶段,可能会出现自闭症/PDD。