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[结节性硬化症中的自闭症]

[Autism in tuberous sclerosis].

作者信息

Calderón González R, Treviño Welsh J, Calderón Sepúlveda A

机构信息

Departamento de Neurología, Instituto de Estudios Neuropediátricos, A.C. Monterrey, N.L.

出版信息

Gac Med Mex. 1994 Sep-Oct;130(5):374-9.

PMID:7607368
Abstract

During the last five years, it has been recognized a very high incidence of autism in children affected by tuberous sclerosis; we believe that this association may be more than just a coincidence and that it may be that the autistic behavior spectrum is related to a great extent, to the anatomic localization of tubers in the frontal and temporoparietal areas. In this study we report our experience with 27 consecutive children, 12 boys and 15 girls with a diagnosis of tuberous sclerosis confirmed by clinical and MRI and or CT findings according to the diagnostic criteria developed by the Diagnosis Criteria Committee of the National Tuberous Sclerosis Association. They were studied during the period of 1988 to 1990. Ages range from 18 months to 16 years (mean: 6.5 years). Twenty-four had epilepsy and were receiving antiepileptic treatment. Seven of the 27 children (25.9 per cent) fulfilled the diagnostic criteria for autistic disorder according to the DSM-III-R. The autistic behavior was evident in all of them by three and half years. The seven children had mental retardation. MRI and CT findings with subependymal calcifications and cortical tubers of frontal and temporoparietal predominance were seen in five of the seven autistic children. In one child, CT was normal and in the other it was not performed. Five were girls and all had West syndrome; two were boys and neither had seizures. Most of the reported cases of children with tuberous sclerosis and autism had experiences West syndrome. In our patients, five of the seven children with autism had west syndrome.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在过去五年中,人们已经认识到结节性硬化症患儿中自闭症的发病率非常高;我们认为这种关联可能不仅仅是巧合,而且自闭症行为谱系在很大程度上可能与额叶和颞顶叶区域的结节解剖定位有关。在本研究中,我们报告了27例连续患儿的情况,其中12名男孩和15名女孩,根据美国国家结节性硬化症协会诊断标准委员会制定的诊断标准,经临床及MRI和/或CT检查确诊为结节性硬化症。他们在1988年至1990年期间接受研究。年龄范围从18个月至16岁(平均:6.5岁)。24例有癫痫并接受抗癫痫治疗。27名患儿中有7名(25.9%)符合DSM-III-R中自闭症障碍的诊断标准。所有患儿在三岁半时自闭症行为均很明显。这7名患儿均有智力发育迟缓。7名自闭症患儿中有5名可见MRI和CT表现为室管膜下钙化以及额叶和颞顶叶为主的皮质结节。1名患儿CT检查正常,另1名未进行CT检查。5名是女孩,均患有韦斯特综合征;2名是男孩,均无癫痫发作。大多数报告的结节性硬化症合并自闭症患儿都有韦斯特综合征病史。在我们的患者中,7名自闭症患儿中有5名患有韦斯特综合征。(摘要截选至250字)

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