Literature DB >> 7833193

Dilated cardiomyopathy due to type II X-linked 3-methylglutaconic aciduria: successful treatment with pantothenic acid.

I Ostman-Smith1, G Brown, A Johnson, J M Land.   

Abstract

A case of dilated cardiomyopathy in a young boy secondary to type II 3-methylglutaconic aciduria is described. A metabolic cause for his dilated cardiomyopathy was suspected because of the development on the electrocardiogram of an unusual "camel's hump" shape of the T waves, and of progressive thickening with increasing echogenicity of the left ventricular wall. He initially improved on digoxin treatment, but did not maintain the response with conventional dietary treatment for this condition. Supplementation with L-carnitine was associated with rapid deterioration in cardiac state, and may be contraindicated in this condition. At a point when the patient was moribund, large doses of pantothenic acid, a precursor of coenzyme A, produced a dramatic and sustained improvement in myocardial function and in growth, neutrophil cell count, hypocholesterolaemia, and hyperuricaemia, which suggests that limitation of availability of coenzyme A is a fundamental pathological process in this condition. The clinical improvement has been maintained for 13 months, and myocardial function is now nearly normal. Oral pantothenol, unlike pantothenic acid, is not efficacious.

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Year:  1994        PMID: 7833193      PMCID: PMC1025545          DOI: 10.1136/hrt.72.4.349

Source DB:  PubMed          Journal:  Br Heart J        ISSN: 0007-0769


  6 in total

1.  Relation of pantothenic acid to adrenal cortical function.

Authors:  E P RALLI; M E DUMM
Journal:  Vitam Horm       Date:  1953       Impact factor: 3.421

2.  Echocardiographic determination of left ventricular mass in man. Anatomic validation of the method.

Authors:  R B Devereux; N Reichek
Journal:  Circulation       Date:  1977-04       Impact factor: 29.690

3.  Hyperuricemia: a marker for cell energy crisis.

Authors:  I H Fox; T D Palella; W N Kelley
Journal:  N Engl J Med       Date:  1987-07-09       Impact factor: 91.245

Review 4.  New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.

Authors:  C A Stanley
Journal:  Adv Pediatr       Date:  1987

5.  Metabolic response to a pantothenic acid deficient diet in humans.

Authors:  P C Fry; H M Fox; H G Tao
Journal:  J Nutr Sci Vitaminol (Tokyo)       Date:  1976       Impact factor: 2.000

6.  X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria.

Authors:  R I Kelley; J P Cheatham; B J Clark; M A Nigro; B R Powell; G W Sherwood; J T Sladky; W P Swisher
Journal:  J Pediatr       Date:  1991-11       Impact factor: 4.406

  6 in total
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1.  Mutation characterization and genotype-phenotype correlation in Barth syndrome.

Authors:  J Johnston; R I Kelley; A Feigenbaum; G F Cox; G S Iyer; V L Funanage; R Proujansky
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 2.  Dilated cardiomyopathy.

Authors:  M Burch; M Runciman
Journal:  Arch Dis Child       Date:  1996-06       Impact factor: 3.791

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Review 5.  The treatment of congenital lactic acidoses.

Authors:  A A Morris; J V Leonard
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Review 7.  X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060).

Authors:  P G Barth; R J Wanders; P Vreken; E A Janssen; J Lam; F Baas
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

Review 8.  Clinical approach to treatable inborn metabolic diseases: an introduction.

Authors:  J-M Saudubray; F Sedel; J H Walter
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9.  Clinical Characteristics and Outcomes of Cardiomyopathy in Barth Syndrome: The UK Experience.

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Review 10.  Barth syndrome.

Authors:  Sarah L N Clarke; Ann Bowron; Iris L Gonzalez; Sarah J Groves; Ruth Newbury-Ecob; Nicol Clayton; Robin P Martin; Beverly Tsai-Goodman; Vanessa Garratt; Michael Ashworth; Valerie M Bowen; Katherine R McCurdy; Michaela K Damin; Carolyn T Spencer; Matthew J Toth; Richard I Kelley; Colin G Steward
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