Literature DB >> 12127323

Newborn mass screening and selective screening using electrospray tandem mass spectrometry in Japan.

Yosuke Shigematsu1, Satoko Hirano, Ikue Hata, Yukie Tanaka, Masakatsu Sudo, Nobuo Sakura, Tsuyoshi Tajima, Seiji Yamaguchi.   

Abstract

Electrospray tandem mass spectrometry was applied to detect a series of inherited metabolic disorders during a newborn-screening pilot study and a selective screening in Japan. In our mass screening of 102,200 newborns, five patients with propionic acidemia, two with methylmalonic acidemia, two with medium-chain acyl-CoA dehydrogenase deficiency, three with citrullinemia type II, and one with phenylketonuria were identified. In a selective screening of 164 patients with symptoms mainly related to hypoglycemia and/or hyperammonemia, 12 with fatty acid oxidation disorders and six with other disorders were found. The results indicated the importance of newborn screening using this technology in Japan. Copyright 2002 Elsevier Science B.V.

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Year:  2002        PMID: 12127323     DOI: 10.1016/s1570-0232(02)00077-6

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  37 in total

1.  Screening of SLC25A13 mutation in the Thai population.

Authors:  Parith Wongkittichote; Chonlaphat Sukasem; Atsuo Kikuchi; Wichai Aekplakorn; Laran T Jensen; Shigeo Kure; Duangrurdee Wattanasirichaigoon
Journal:  World J Gastroenterol       Date:  2013-11-21       Impact factor: 5.742

Review 2.  Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management.

Authors:  Prem S Shekhawat; Dietrich Matern; Arnold W Strauss
Journal:  Pediatr Res       Date:  2005-04-06       Impact factor: 3.756

3.  Useful second-tier tests in expanded newborn screening of isovaleric acidemia and methylmalonic aciduria.

Authors:  Yosuke Shigematsu; Ikue Hata; Go Tajima
Journal:  J Inherit Metab Dis       Date:  2010-05-04       Impact factor: 4.982

4.  Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry.

Authors:  Lianshu Han; Feng Han; Jun Ye; Wenjuan Qiu; Huiwen Zhang; Xiaolan Gao; Yu Wang; Wenjun Ji; Xuefan Gu
Journal:  J Clin Lab Anal       Date:  2014-05-05       Impact factor: 2.352

Review 5.  Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspective.

Authors:  William J Rhead
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

6.  Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency.

Authors:  Yao Bang Lu; Keiko Kobayashi; Miharu Ushikai; Ayako Tabata; Mikio Iijima; Meng Xian Li; Lei Lei; Kotaro Kawabe; Satoru Taura; Yanling Yang; Tze-Tze Liu; Szu-Hui Chiang; Kwang-Jen Hsiao; Yu-Lung Lau; Lap-Chee Tsui; Dong Hwan Lee; Takeyori Saheki
Journal:  J Hum Genet       Date:  2005-07-30       Impact factor: 3.172

7.  Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse.

Authors:  Naomi van Vlies; Liqun Tian; Henk Overmars; Albert H Bootsma; Willem Kulik; Ronald J A Wanders; Philip A Wood; Frédéric M Vaz
Journal:  Biochem J       Date:  2005-04-01       Impact factor: 3.857

8.  The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity.

Authors:  T Fukao; G X Zhang; N Sakura; T Kubo; H Yamaga; A Hazama; Y Kohno; N Matsuo; M Kondo; S Yamaguchi; Y Shigematsu; N Kondo
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

9.  Detection of Inborn Errors of Metabolism using Tandem Mass Spectrometry among High-risk Omani Patients.

Authors:  Sulaiman Al Riyami; Matar Al Maney; Surendra Nath Joshi; Riad Bayoumi
Journal:  Oman Med J       Date:  2012-11

10.  Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia.

Authors:  Faiqa Imtiaz; Bashayer M Al-Mubarak; Abeer Al-Mostafa; Mohamed Al-Hamed; Rabab Allam; Zuhair Al-Hassnan; Mohammed Al-Owain; Hamad Al-Zaidan; Zuhair Rahbeeni; Alya Qari; Eissa Ali Faqeih; Ali Alasmari; Fuad Al-Mutairi; Majid Alfadhel; Wafaa M Eyaid; Mohamed S Rashed; Moeenaldeen Al-Sayed
Journal:  JIMD Rep       Date:  2015-11-29
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