Literature DB >> 19904473

Outcome of organic acidurias in China.

Yanling Yang1, Zhang Yao, Jinqing Song, Yuki Hasegawa, Masahiko Kimura, Seiji Yamaguchi, Yuwu Jiang, Jiong Qin, Xiru Wu.   

Abstract

From June 1998 to May 2007, 9566 urine samples were collected from patients with psychomotor deficits, seizures, vomiting and unconsciousness in Peking University First Hospital. Their urine organic acids profiles were analysed using gas chromatography - mass spectrometry (GCMS), GCMS solution and Inborn Errors of Metabolism Screening System software. In all patients, blood acylcarnitines were analysed using tandem mass spectrometry. One hundred and sixty-eight patients (1.76%) with organic acidurias were detected. Among them, 116 (116/ 168, 69.0%) had methylmalonic aciduria, 63 (54.3%) of these 116 patients had methylmalonic aciduria combined with homocysteinemia. Sixteen (9.5%) of those patients detected with organic acidurias had propionic aciduria, and 15 (8.9%) had multiple carboxylase deficiency. Seven (4.2%) had glutaric aciduria type 1. After dietary treatment, medicine and rehabilitation, clinical improvements were observed in more than half of the patients. Twenty-eight of the 168 patients (16.7%) recovered and led a normal life. The method of urine organic acid analysis by gas chromatography - mass spectrometry and blood acylcarnitines analysis by tandem mass spectrometry have been established and applied successfully in China, namely Beijing, Shanghai, Wuhan and Guangzhou. The prognoses of Chinese patients with organic acidurias have also improved significantly.

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Year:  2008        PMID: 19904473

Source DB:  PubMed          Journal:  Ann Acad Med Singap        ISSN: 0304-4602            Impact factor:   2.473


  4 in total

1.  The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism.

Authors:  Jamiyan Purevsuren; Baasandai Bolormaa; Chogdon Narantsetseg; Renchindorj Batsolongo; Ochirbat Enkhchimeg; Munkhuu Bayalag; Yuki Hasegawa; Haruo Shintaku
Journal:  Mol Genet Metab Rep       Date:  2016-10-28

2.  Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.

Authors:  Naoaki Shibata; Yuki Hasegawa; Kenji Yamada; Hironori Kobayashi; Jamiyan Purevsuren; Yanling Yang; Vu Chi Dung; Nguyen Ngoc Khanh; Ishwar C Verma; Sunita Bijarnia-Mahay; Dong Hwan Lee; Dau-Ming Niu; Georg F Hoffmann; Yosuke Shigematsu; Toshiyuki Fukao; Seiji Fukuda; Takeshi Taketani; Seiji Yamaguchi
Journal:  Mol Genet Metab Rep       Date:  2018-05-21

3.  Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings.

Authors:  Yiming Lin; Chunmei Lin; Weihua Lin; Zhenzhu Zheng; Mingya Han; Qingliu Fu
Journal:  BMC Med Genet       Date:  2018-07-11       Impact factor: 2.103

4.  Segmental uniparental disomy of chromosome 4 in a patient with methylmalonic acidemia.

Authors:  Min Chen; Hu Hao; Hui Xiong; Yao Cai; Fei Ma; Congcong Shi; Xin Xiao; Sitao Li
Journal:  Mol Genet Genomic Med       Date:  2019-12-02       Impact factor: 2.183

  4 in total

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