Literature DB >> 11295726

Carnitine transporter defect diagnosed by newborn screening with electrospray tandem mass spectrometry.

B Wilcken1, V Wiley, K G Sim, K Carpenter.   

Abstract

The carnitine transporter defect is a potentially fatal but treatable disorder. We used electrospray tandem mass spectrometry in the New South Wales (Australia) Newborn Screening Programme to measure free carnitine and acylcarnitine species in the newborn population. Free carnitine levels in dried blood samples from 149,000 neonates did not vary markedly between 2 and 8 days of age. Two of 4 babies subsequently diagnosed clinically with the carnitine transporter defect had a free carnitine level in the neonatal blood sample low enough to be detected by screening.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11295726     DOI: 10.1067/mpd.2001.111813

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  25 in total

1.  Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands.

Authors:  Jan Rasmussen; Olav W Nielsen; Nils Janzen; Morten Duno; Hannes Gislason; Lars Køber; Ulrike Steuerwald; Allan M Lund
Journal:  J Inherit Metab Dis       Date:  2013-05-08       Impact factor: 4.982

2.  Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency.

Authors:  M Kilic; R K Ozgül; T Coşkun; D Yücel; M Karaca; H S Sivri; A Tokatli; M Sahin; T Karagöz; A Dursun
Journal:  JIMD Rep       Date:  2011-09-22

3.  Identification of two novel mutations in OCTN2 from two Saudi patients with systemic carnitine deficiency.

Authors:  Z Rahbeeni; F M Vaz; K Al-Hussein; M P Bucknall; J Ruiter; R J Wanders; M S Rashed
Journal:  J Inherit Metab Dis       Date:  2002-09       Impact factor: 4.982

4.  Genotype-phenotype correlation in primary carnitine deficiency.

Authors:  Emily C Rose; Cristina Amat di San Filippo; Uzochi C Ndukwe Erlingsson; Orly Ardon; Marzia Pasquali; Nicola Longo
Journal:  Hum Mutat       Date:  2011-10-11       Impact factor: 4.878

5.  Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death.

Authors:  Najim Lahrouchi; Elisabeth M Lodder; Maria Mansouri; Rafik Tadros; Layla Zniber; Najlae Adadi; Sally-Ann B Clur; Karin Y van Spaendonck-Zwarts; Alex V Postma; Abdelaziz Sefiani; Ilham Ratbi; Connie R Bezzina
Journal:  Eur J Hum Genet       Date:  2017-03-15       Impact factor: 4.246

Review 6.  Disorders of carnitine transport and the carnitine cycle.

Authors:  Nicola Longo; Cristina Amat di San Filippo; Marzia Pasquali
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-05-15       Impact factor: 3.908

7.  Dilated Cardiomyopathy as the Only Clinical Manifestation of Carnitine Transporter Deficiency.

Authors:  Kyriaki Papadopoulou-Legbelou; Maria Gogou; Vaia Dokousli; Maria Eboriadou; Athanasios Evangeliou
Journal:  Indian J Pediatr       Date:  2016-11-03       Impact factor: 1.967

8.  Fatty Acid oxidation disorders in a chinese population in taiwan.

Authors:  Yin-Hsiu Chien; Ni-Chung Lee; Mei-Chyn Chao; Li-Chu Chen; Li-Hsin Chen; Chun-Ching Chien; Hui-Chen Ho; Jeng-Hung Suen; Wuh-Liang Hwu
Journal:  JIMD Rep       Date:  2013-05-23

9.  Transport of butyryl-L-carnitine, a potential prodrug, via the carnitine transporter OCTN2 and the amino acid transporter ATB(0,+).

Authors:  Sonne R Srinivas; Puttur D Prasad; Nagavedi S Umapathy; Vadivel Ganapathy; Prem S Shekhawat
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2007-09-13       Impact factor: 4.052

10.  Cardiomyopathy and carnitine deficiency.

Authors:  Cristina Amat di San Filippo; Matthew R G Taylor; Luisa Mestroni; Lorenzo D Botto; Nicola Longo
Journal:  Mol Genet Metab       Date:  2008-03-11       Impact factor: 4.797

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.