Literature DB >> 15243991

The early-onset phenotype of mitochondrial trifunctional protein deficiency: a lethal disorder with multiple tissue involvement.

U Spierkerkoetter1, Z Khuchua, Z Yue, A W Strauss.   

Abstract

Mitochondrial trifunctional protein (TFP) deficiency is a clinically heterogeneous disorder with phenotypes of different severity. Early onset, severe forms predominantly exhibit cardiomyopathy, life-threatening arrhythmias and liver dysfunction; the later-onset, milder phenotype is mainly characterized by neuromyopathic features. The mechanisms that determine these heterogeneous presentations are unknown. We performed multiple tissue immunoblots from a patient with early-onset, lethal TFP deficiency and demonstrated absent TFP antigen in all. The predominant cardiac manifestation of severe TFP deficiency reflects its essential role in myocardial energetics, not its tissue-specific expression.

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Year:  2004        PMID: 15243991     DOI: 10.1023/b:boli.0000028839.57386.88

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  6 in total

Review 1.  Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening.

Authors:  Ute Spiekerkoetter
Journal:  J Inherit Metab Dis       Date:  2010-05-07       Impact factor: 4.982

Review 2.  Current issues regarding treatment of mitochondrial fatty acid oxidation disorders.

Authors:  Ute Spiekerkoetter; Jean Bastin; Melanie Gillingham; Andrew Morris; Frits Wijburg; Bridget Wilcken
Journal:  J Inherit Metab Dis       Date:  2010-09-10       Impact factor: 4.982

3.  Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases.

Authors:  Ryosuke Bo; Kenji Yamada; Hironori Kobayashi; Purevsuren Jamiyan; Yuki Hasegawa; Takeshi Taketani; Seiji Fukuda; Ikue Hata; Yo Niida; Yosuke Shigematsu; Kazumoto Iijima; Seiji Yamaguchi
Journal:  J Hum Genet       Date:  2017-05-18       Impact factor: 3.172

4.  The trifunctional protein mediates thyroid hormone receptor-dependent stimulation of mitochondria metabolism.

Authors:  E Sandra Chocron; Naomi L Sayre; Deborah Holstein; Nuttawut Saelim; Jamal A Ibdah; Lily Q Dong; Xuguang Zhu; Sheue-Yann Cheng; James D Lechleiter
Journal:  Mol Endocrinol       Date:  2012-05-08

5.  A fetus with mitochondrial trifunctional protein deficiency: Elevation of 3-OH-acylcarnitines in amniotic fluid functionally assured the genetic diagnosis.

Authors:  Ryosuke Bo; Yuki Hasegawa; Kenji Yamada; Hironori Kobayashi; Takeshi Taketani; Seiji Fukuda; Seiji Yamaguchi
Journal:  Mol Genet Metab Rep       Date:  2015-12-05

Review 6.  Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease.

Authors:  Abena Nsiah-Sefaa; Matthew McKenzie
Journal:  Biosci Rep       Date:  2016-02-02       Impact factor: 3.840

  6 in total

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