Skip to
  1. Homepage
  2. Rare diseases
  3. Search
Simple search

Simple search

*
(*) mandatory field





 

Other search option(s)

Very long chain acyl-CoA dehydrogenase deficiency

Orpha number ORPHA26793
Synonym(s) VLCAD deficiency
VLCADD
Prevalence 1-9 / 100 000
Inheritance Autosomal recessive
Age of onset Neonatal
Infancy
ICD-10
  • E71.3
ICD-O -
OMIM
UMLS -
MeSH -
MedDRA -

Summary

Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency (VLCADD) is an inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis.

Over 400 cases have been reported worldwide. Prevalence in Germany is of 1/50, 000.

VLCADD is a clinically heterogeneous disease, with 3 major phenotypes. Severe infantile VLCADD has an early onset, usually within the first 3-12 months of life and as early as the neonatal period, with high mortality and a high incidence of hypoketotic hypoglycaemia, liver disease, cardiac arrhythmias and cardiomyopathy. Pericardial effusion is also reported. Moderately severe infantile/childhood VLCADD has a later onset (early neonatal period to early childhood) and usually presents with hypoketotic hypoglycemia, lower mortality and rarely cardiomyopathy. Late-onset myopathic VLCADD presents in older children and young adults (usually >10 years of age) with isolated skeletal muscle involvement, exercise intolerance, myalgia, rhabdomyolysis and myoglobinuria usually triggered by exercise, fasting, cold/heat and/or stress but viral infection can also precipitate/exacerbate this presentation. In rare cases it can lead to renal failure and can be fatal. Some patients presenting with myopathic disease may have a previous history of hypoglycemia in infancy/childhood.

VLCADD is caused by mutations in the ACADVL gene (17p13.1). Mutations of this gene lead to dysfunction of mitochondrial beta-oxidation of long-chain fatty acids.

Abnormal plasma or blood acylcarnitine profile identifies virtually all patients with the severe/moderately severe phenotypes by demonstrating increased C14:1 and C14:1/C12:1 ratios together with elevations of C12, C16, C16:1, C18 and C18:1 species. Occasionally patients with mainly myopathic disease can give an essentially normal profile when metabolically stable. Crisis urine organic acid analysis generally shows a non-specific abnormal pattern of C6-C14 dicarboxylic and hydroxydicarboxylic acids. Newborn screening is available in Austria, Czech Republic, Denmark, Germany, Hungary, Iceland, Netherlands, Portugal and Spain (milder ''late-onset'' patients may not be detected). VLCADD is confirmed by showing two pathogenic mutations in the ACADVL gene. Fatty acid oxidation flux assays in cultured fibroblasts or direct measurement of VLCAD activity in lymphocytes or fibroblasts can also clarify difficult diagnoses.

Differential diagnosis includes other long chain fat oxidation defects. Myopathic carnitine palmitoyl transferase II deficiency (see this term) has a presentation identical to the myopathic presentation of VLCADD.

Antenatal diagnosis is possible when mutation(s) have been identified within the family.

VLCADD is inherited autosomal recessively and genetic counseling is available.

Dietary treatment along with strict avoidance of fasting is essential in infants/children and involves a low long-chain fat diet in combination with medium chain triglycerides. An emergency regimen should be available for each patient to use when they cannot tolerate their prescribed diet. Medical treatment should be sought immediately if there is evidence of decompensation. Those with a milder phenotype should limit exercise and cold/heat exposure and avoid fasting. Treatment with bezafibrate offers potential benefit in myopathic patients with residual enzyme activity, although this awaits full clinical evaluation.

VLCADD can be fatal but thanks to newborn screening programs, the outcome is improving for all phenotypes. Prognosis is much better for milder phenotypes provided that there is adherence to treatment protocols.

Expert reviewer(s)

  • Dr Simon OLPIN

(*) Required fields.

Attention: Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.


Captcha image

Detailed information

Emergency guidelines
  • EN (2012,pdf)
Clinical genetics review
  • EN (2014)
Get Acrobat Reader
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.