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在经过选择性筛查的特发性智力障碍人群中检测代谢紊乱情况。

Detection of metabolic disorders among selectively screened people with idiopathic mental retardation.

作者信息

Kurtz M B, Finucane B, Hyland K, Bottiglieri T, Sherwood W G, Bennett M J

机构信息

Genetic Services, Elwyn, Inc., PA 19063.

出版信息

Ment Retard. 1994 Oct;32(5):328-33.

PMID:7984117
Abstract

Fifth-eight people receiving residential or other services for idiopathic mental retardation were evaluated for evidence of metabolic disease. Five (8%) demonstrated persistent urinary organic acid abnormalities on at least three occasions, which pointed towards specific genetic metabolic defects. Instigation of specific treatment programs may have improved the quality of life for one of these participants. Appropriate genetic counseling was provided but could have been instigated much earlier had these investigations been performed as part of a routine workup for idiopathic mental retardation. This pilot study suggests a need for evaluation of other similar populations with idiopathic mental retardation.

摘要

对58名因特发性智力迟钝而接受住院或其他服务的患者进行了代谢疾病证据评估。5人(8%)至少在三次检测中出现持续性尿有机酸异常,这指向特定的遗传代谢缺陷。对其中一名参与者实施特定治疗方案可能改善了其生活质量。已提供适当的遗传咨询,但如果这些检查作为特发性智力迟钝常规检查的一部分进行,咨询本可更早开展。这项初步研究表明,有必要对其他类似的特发性智力迟钝人群进行评估。

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