Literature DB >> 11048739

Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center.

C Zhang1, K Xu, U P Dave, Y Wang, I Matsumoto.   

Abstract

To heighten the effectiveness of chemical diagnosis for inborn errors of metabolism (IEM) using urease pretreatment and GC-MS analysis, a sample collection and transportation method was contrived. The resulting "filter paper set" allows simple urine collection and transportation, and enables anyone from anywhere to receive the GC-MS analysis without the limitations of place or time. Using filter paper sets, high-risk screening of undiagnosed children or mentally retarded children with unknown cause was conducted in cooperation with hospitals and universities in several Asian countries. During 8 months 203 patients from China and India were analyzed and 20 cases of IEM were chemically diagnosed. These diagnoses greatly contributed to the treatment of children with intractable diseases who lived in Asian countries where analytical techniques and facilities for IEM were not sufficient.

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Year:  2000        PMID: 11048739     DOI: 10.1016/s0378-4347(00)00087-6

Source DB:  PubMed          Journal:  J Chromatogr B Biomed Sci Appl        ISSN: 1387-2273


  6 in total

1.  The Comparison of Iodine-Type and MnO2-Type Oxidation for Measuring the Levels of Urine Neopterin and Biopterin in Patients with Hyperphenylalaninemia: A Descriptive-Analytic Study in Iran.

Authors:  Atena Askarizadeh; Shohreh Khatami; Soghra Rouhi Dehnabeh
Journal:  Indian J Clin Biochem       Date:  2018-08-23

2.  Multiple Acyl-CoA Dehydrogenation Deficiency (Glutaric Aciduria Type II) with a Novel Mutation of Electron Transfer Flavoprotein-Dehydrogenase in a Cat.

Authors:  Shoichi Wakitani; Shidow Torisu; Taiki Yoshino; Kazuhisa Hattanda; Osamu Yamato; Ryuji Tasaki; Haruo Fujita; Koichiro Nishino
Journal:  JIMD Rep       Date:  2013-10-20

3.  Study of inborn errors of metabolism in urine from patients with unexplained mental retardation.

Authors:  Angela Sempere; Angela Arias; Guillermo Farré; Judith García-Villoria; Pilar Rodríguez-Pombo; Lurdes R Desviat; Begoña Merinero; Angels García-Cazorla; Maria A Vilaseca; Antonia Ribes; Rafael Artuch; Jaume Campistol
Journal:  J Inherit Metab Dis       Date:  2010-01-05       Impact factor: 4.982

4.  Inborn Errors of Metabolism in Children with Unexplained Developmental Delay in Misan, Iraq.

Authors:  Hassan A Altimimi; Hussein F Aljawadi; Esraa A Ali
Journal:  Oman Med J       Date:  2019-07

5.  Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome.

Authors:  Junling Wang; Zhimei Liu; Manting Xu; Xiaodi Han; Changhong Ren; Xinying Yang; Chunhua Zhang; Fang Fang
Journal:  Front Pharmacol       Date:  2021-03-08       Impact factor: 5.810

6.  Case Report: A Novel Missense Mutation c.517G>C in the UMPS Gene Associated With Mild Orotic Aciduria.

Authors:  Rui Ma; Jing Ye; Jiaqi Han; Lehong Gao; Chaodong Wang; Yuping Wang
Journal:  Front Neurol       Date:  2022-03-09       Impact factor: 4.003

  6 in total

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