Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Sep;38(5):881-7.
doi: 10.1007/s10545-014-9804-6. Epub 2015 Jan 20.

Fructose 1,6-bisphosphatase deficiency: clinical, biochemical and genetic features in French patients

Affiliations

Fructose 1,6-bisphosphatase deficiency: clinical, biochemical and genetic features in French patients

Elise Lebigot et al. J Inherit Metab Dis. 2015 Sep.

Abstract

Fructose-1,6-bisphosphatase (FBPase) deficiency is a very rare autosomal recessive disorder caused by a mutation of the fructose-1,6-bisphosphatase gene(FBP1). Disease is mainly revealed by hypoglycemia and lactic acidosis, both symptoms being characteristic for an enzymatic block in the last steps of the gluconeogenesis. Twelve patients with FBPase deficiency were diagnosed in France in the 2001-2013 period, using a diagnostic system based on a single blood sample which allows simultaneous enzyme activity measurement on mononuclear white blood cells and molecular analysis. Sequencing of exons and intron-exon junctions of FBP1 gene was completed in unsolved cases by a gene dosage assay developed for each exon. For most patients, first metabolic decompensation occurred before two years of age with a similar sequence: the triggering factors were fever, fasting, or decrease of food intake. However, diagnosis was made late at a mean age of 3 years, as mitochondrial defects or glycogen storage diseases were firstly suspected. Enzyme activity in leukocytes was dramatically decreased (<10%). Twelve different mutations were identified in 22 alleles among them seven were novels: one missense mutation c.472C > T, one point deletion c.48del, one point duplication c.865dupA, one deletion-insertion, and two splice mutations (c.427-1del and c.825 + 1G > A). We described the first intragenic deletion in FBP1 (g.97,364,754_97,382,011del) in homozygous state. Our report also confirms that this very rare disease is misdiagnosed, as other energetic defects are firstly suspected.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Inherit Metab Dis. 2001 Feb;24(1):87-8 - PubMed
    1. Eur J Pediatr. 2013 Sep;172(9):1249-53 - PubMed
    1. Clin Chim Acta. 1982 Feb 26;119(1-2):143-8 - PubMed
    1. Genomics. 1995 Jun 10;27(3):520-5 - PubMed
    1. Ugeskr Laeger. 2006 Nov 13;168(46):4014-5 - PubMed

LinkOut - more resources