Literature DB >> 9290621

Sudden neonatal death in carnitine transporter deficiency.

P Rinaldo1, C A Stanley, B Y Hsu, L A Sanchez, H J Stern.   

Abstract

A newborn infant died suddenly and unexpectedly on day 5 of life. Postmortem investigations led to a suspicion of carnitine transporter deficiency, a diagnosis supported by the finding that both parents are heterozygotes for this disorder. The fasting stress caused by poor breast-feeding with no formula supplements and, possibly, the vegetarian diet of the mother were likely the critical factors leading to neonatal death, an outcome previously not described in this disorder.

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Year:  1997        PMID: 9290621     DOI: 10.1016/s0022-3476(97)70171-9

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


  14 in total

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Authors:  Harjot K Saini-Chohan; Ryan W Mitchell; Frédéric M Vaz; Teresa Zelinski; Grant M Hatch
Journal:  J Lipid Res       Date:  2011-11-07       Impact factor: 5.922

2.  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

3.  Successful perioperative management of a patient with primary systemic carnitine deficiency: a case report.

Authors:  Karin Kato; Toshiyuki Mizota; Kiichi Hirota; Kazuhiko Fukuda
Journal:  J Anesth       Date:  2012-09-21       Impact factor: 2.078

4.  Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency.

Authors:  Y Wang; J Ye; V Ganapathy; N Longo
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

Review 5.  Defects in activation and transport of fatty acids.

Authors:  M Brivet; A Boutron; A Slama; C Costa; L Thuillier; F Demaugre; D Rabier; J M Saudubray; J P Bonnefont
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

6.  Performance of Expanded Newborn Screening in Norway Supported by Post-Analytical Bioinformatics Tools and Rapid Second-Tier DNA Analyses.

Authors:  Trine Tangeraas; Ingjerd Sæves; Claus Klingenberg; Jens Jørgensen; Erle Kristensen; Gunnþórunn Gunnarsdottir; Eirik Vangsøy Hansen; Janne Strand; Emma Lundman; Sacha Ferdinandusse; Cathrin Lytomt Salvador; Berit Woldseth; Yngve T Bliksrud; Carlos Sagredo; Øyvind E Olsen; Mona C Berge; Anette Kjoshagen Trømborg; Anders Ziegler; Jin Hui Zhang; Linda Karlsen Sørgjerd; Mari Ytre-Arne; Silje Hogner; Siv M Løvoll; Mette R Kløvstad Olavsen; Dionne Navarrete; Hege J Gaup; Rina Lilje; Rolf H Zetterström; Asbjørg Stray-Pedersen; Terje Rootwelt; Piero Rinaldo; Alexander D Rowe; Rolf D Pettersen
Journal:  Int J Neonatal Screen       Date:  2020-06-27

Review 7.  Inborn errors of energy metabolism associated with myopathies.

Authors:  Anibh M Das; Ulrike Steuerwald; Sabine Illsinger
Journal:  J Biomed Biotechnol       Date:  2010-05-26

Review 8.  Carnitine transport: pathophysiology and metabolism of known molecular defects.

Authors:  I Tein
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

9.  Glucose-free medium exacerbates microvesicular steatosis in cultured skin fibroblasts of genetic defects of fatty acid oxidation. A novel screening test.

Authors:  D L Renaud; V Edwards; G J Wilson; I Tein
Journal:  J Inherit Metab Dis       Date:  2002-11       Impact factor: 4.982

10.  Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5q.

Authors:  Y Shoji; A Koizumi; T Kayo; T Ohata; T Takahashi; K Harada; G Takada
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

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