Literature DB >> 23868323

Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.

Teerin Liewluck1, Manpreet S Mundi, Michelle L Mauermann.   

Abstract

INTRODUCTION: Mitochondrial trifunctional protein deficiency is a rare autosomal recessive disorder of mitochondrial fatty acid β-oxidation that may be due to mutations in 2 different nuclear genes, HADHA and HADHB. Perturbation of this multienzyme complex compromises the oxidation of long-chain fatty acids, which leads to multiorgan dysfunction. Childhood- or adolescent-onset recurrent rhabdomyolysis is a common muscular manifestation and is preceded frequently by clinically overt peripheral neuropathy.
METHODS: In this report we describe a patient with late adult-onset recurrent rhabdomyolysis.
RESULTS: Despite normal sensory examination, nerve conduction studies showed a mild axonal peripheral neuropathy. The acylcarnitine profile showed elevated long-chain and 3-hydroxy long-chain acylcarnitine species. HADHA sequencing revealed known compound heterozygous mutations c.180+3A>G (p.Thr37SerfsX6) and c.1528G>C (p.Glu510Gln). During a 10-month follow-up period, he had no further episodes of rhabdomyolysis after appropriate dietary modifications.
CONCLUSIONS: Mitochondrial trifunctional protein deficiency should be considered in patients with adult-onset recurrent rhabdomyolysis, especially in those with either clinically overt or subclinical peripheral neuropathy.
Copyright © 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  HADHA; HADHB; long-chain fatty acid; mitochondrial trifunctional protein deficiency; peripheral neuropathy; rhabdomyolysis

Mesh:

Substances:

Year:  2013        PMID: 23868323     DOI: 10.1002/mus.23959

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  4 in total

1.  Diagnostic evaluation of rhabdomyolysis.

Authors:  Jessica R Nance; Andrew L Mammen
Journal:  Muscle Nerve       Date:  2015-03-14       Impact factor: 3.217

2.  A novel HADHA variant associated with an atypical moderate and late-onset LCHAD deficiency.

Authors:  Anne-Frédérique Dessein; Eléonore Hebbar; Joseph Vamecq; Elodie Lebredonchel; Aurore Devos; Jamal Ghoumid; Karine Mention; Dries Dobbelaere; Marie Joncquel Chevalier-Curt; Monique Fontaine; Sabine Defoort; Vassily Smirnov; Claire Douillard; Claire-Marie Dhaenens
Journal:  Mol Genet Metab Rep       Date:  2022-03-15

Review 3.  Rhabdomyolysis: a genetic perspective.

Authors:  Renata Siciliani Scalco; Alice R Gardiner; Robert Ds Pitceathly; Edmar Zanoteli; Jefferson Becker; Janice L Holton; Henry Houlden; Heinz Jungbluth; Ros Quinlivan
Journal:  Orphanet J Rare Dis       Date:  2015-05-02       Impact factor: 4.123

4.  Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosis.

Authors:  Nils Janzen; Alejandro D Hofmann; Gunnar Schmidt; Anibh M Das; Sabine Illsinger
Journal:  Orphanet J Rare Dis       Date:  2017-12-21       Impact factor: 4.123

  4 in total

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