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自闭症谱系障碍和先天性代谢缺陷:最新进展。

Autism spectrum disorders and inborn errors of metabolism: an update.

机构信息

University of Michigan, Ann Arbor, Michigan, and King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

出版信息

Pediatr Neurol. 2013 Oct;49(4):232-6. doi: 10.1016/j.pediatrneurol.2013.05.013. Epub 2013 Aug 3.

Abstract

BACKGROUND

Autism spectrum disorder is characterized by social communicative deficits with restricted interests occurring in about 1% of the population. Although its exact cause is not known, several factors have been implicated in its etiology, including inborn errors of metabolism. Although relatively uncommon, these disorders frequently occur in countries with high rates of consanguinity and are often associated with behavioral problems, such as hyperactivity and aggression. The aim of this review is to examine the association of autism with these conditions.

METHOD

A computer-assisted search was performed to identify the most common inborn errors of metabolism associated with autism.

RESULTS

The following disorders were identified: phenylketonuria, glucose-6-phosphatase deficiency, propionic acidemia, adenosine deaminase deficiency, Smith-Lemli-Opitz syndrome and mitochondrial disorders, and the recently described branched chain ketoacid dehydrogenase kinase deficiency.

CONCLUSION

The risk of autistic features is increased in children with inborn errors of metabolism, especially in the presence of cognitive and behavioral deficits. We propose that affected children should be screened for autism.

摘要

背景

自闭症谱系障碍的特征是社交沟通障碍,伴有受限的兴趣,发生在大约 1%的人群中。尽管其确切原因尚不清楚,但有几个因素与自闭症的病因有关,包括先天性代谢缺陷。尽管这些疾病相对少见,但在高近亲结婚率的国家经常发生,并且常与行为问题有关,如多动和攻击行为。本综述的目的是研究自闭症与这些情况的关联。

方法

通过计算机辅助搜索确定与自闭症相关的最常见的先天性代谢缺陷。

结果

确定了以下疾病:苯丙酮尿症、葡萄糖-6-磷酸酶缺乏症、丙酸血症、腺苷脱氨酶缺乏症、Smith-Lemli-Opitz 综合征和线粒体疾病,以及最近描述的支链酮酸脱氢酶激酶缺乏症。

结论

患有先天性代谢缺陷的儿童患自闭症特征的风险增加,尤其是在存在认知和行为缺陷的情况下。我们建议对受影响的儿童进行自闭症筛查。

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