[重度智力发育迟缓儿童群体代谢紊乱研究的进一步结果（2）]

[Further results of studies on metabolic disorders in a population of severely retarded children (2)].

作者信息

Opałka S, Galewicz A, Pisarska E, Wegrzynowicz Z

出版信息

Psychiatr Neurol Med Psychol Beih. 1968;8-9:126-9.

Abstract

The purpose of this work was to analyse amino-acids in urine of mentally handicapped children and concentration of amino-acids in urine. Undesalted, night urine was investigated by two dimensional ascending chromatography method. Preliminary results show a great variety of composition from 6 to 23 amino-acids and pathological amino-acids excretion in 14% cases. Besides normal presented amino-acids in urine it was till now detected 3.5% cases of phenylketonuria, 1.5% cases of prolinuria and 24% cases of amino-butyric-acids excretion.

摘要

这项工作的目的是分析智障儿童尿液中的氨基酸及尿液中氨基酸的浓度。采用双向上升色谱法对未脱盐的夜间尿液进行研究。初步结果显示，尿液中氨基酸组成种类繁多，有6至23种，14%的病例存在病理性氨基酸排泄。除了尿液中正常存在的氨基酸外，目前还检测到3.5%的苯丙酮尿症病例、1.5%的脯氨酸尿症病例以及24%的γ-氨基丁酸排泄病例。

相似文献

1

[Further results of studies on metabolic disorders in a population of severely retarded children (2)].[重度智力发育迟缓儿童群体代谢紊乱研究的进一步结果（2）]

Psychiatr Neurol Med Psychol Beih. 1968;8-9:126-9.

2

Screening for inborn errors of amino acid metabolism.氨基酸代谢先天性疾病的筛查。

Ann Clin Lab Sci. 1991 Mar-Apr;21(2):123-42.

3

[Patterns of urinary aminoacid excretion in exceptional children and patients with mental disorders in Costa Rica].[哥斯达黎加特殊儿童和精神障碍患者的尿氨基酸排泄模式]

Rev Biol Trop. 1983 Jun;31(1):1-9.

4

The Vodskov project. 3. Thin-layer chromatography of amino acids in urine from mentally retarded patients. Methodology of the investigation.沃兹科夫项目。3. 智障患者尿液中氨基酸的薄层色谱法。调查方法。

Dan Med Bull. 1969 Sep;16(8):235-8.

5

The Vodskov project 5: thin layer chromatography of amino acids in urine from mentally retarded patients. Repeat investigations of the cases of aminoaciduria found in the primary investigation.

Dan Med Bull. 1970 Jan;17(1):1-7.

6

High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.用于确认马来西亚先天性代谢缺陷儿童薄层色谱（TLC）检测结果的高效液相色谱（HPLC）方法。

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:130-3.

7

[Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].[氨基酸代谢紊乱诊断中的临床定位尝试。I. 泌尿系统症状、神经精神症状和眼部症状]

Presse Med (1893). 1968 Apr 20;76(19):903-6.

8

[Systematic detection of hereditary metabolic encephalopathies].

Ann Pediatr (Paris). 1968 Oct 2;15(10):635-41.

9

Urinary excretion of aminoacids in mentally retarded children. A study of 150 cases by circular paper chromatography.智障儿童氨基酸的尿排泄情况。采用圆形纸色谱法对150例病例的研究。

Neurol India. 1970 Mar;18(1):17-21.

10

Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population.正常人群和智力发育迟缓人群中苯丙酮尿症及其他先天性氨基酸代谢紊乱的发病率。

Rev Czech Med. 1974;20(1):18-22.

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