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
. 2017:35:33-37.
doi: 10.1007/8904_2016_21. Epub 2016 Nov 30.

Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine

Affiliations

Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine

Gerarda Cappuccio et al. JIMD Rep. 2017.

Abstract

We report three patients with elevations of propionylcarnitine (C3), one without elevations of 2-methylcitrate and 3-hydroxypropionate in urine organic acid analysis, and the other two showing only mild elevations, all of whom were subsequently confirmed to have propionic acidemia by molecular analysis of PCCA and PCCB genes. To date, they have had a mild clinical course. These cases illustrate the importance of considering high C3 as the only biochemical abnormality in a diagnosis of propionic acidemia. Since mild C3 elevations may be overlooked and considered non-diagnostic in isolation, we advise considering a diagnosis of propionic acidemia even in the absence of significant elevations 2-methylcitrate or 3-hydroxypropionate in urine organic acid analysis.

Keywords: 2-Methylcitrate; 3-Hydroxypropionate; Acyl-carnitine; Atypical Phenotype; C3; Propionic acidemia.

PubMed Disclaimer

References

    1. Al-Dirbashi OY, McIntosh N, McRoberts C, Fisher L, Rashed MS, Makhseed N, Geraghty MT, Santa T, Chakraborty P. Analysis of methylcitrate in dried blood spots by liquid chromatography-tandem mass spectrometry. JIMD Rep. 2014;16:65. doi: 10.1007/8904_2014_321. - DOI - PMC - PubMed
    1. Campeau E, Desviat LR, Leclerc D, Wu X, Pérez B, Ugarte M, Gravel RA. Structure of the PCCA gene and distribution of mutations causing propionic acidemia. Mol Genet Metab. 2001;74:238–247. doi: 10.1006/mgme.2001.3210. - DOI - PubMed
    1. Campeau E, Dupuis L, León-Del-Rio A, Gravel R. Coding sequence mutations in the alpha subunit of propionyl-CoA Carboxylase in patients with propionic acidemia. Mol Genet Metab. 1999;67:11–22. doi: 10.1006/mgme.1999.2850. - DOI - PubMed
    1. Desviat LR, Clavero S, Perez-Cerdá C, Navarrete R, Ugarte M, Perez B. New splicing mutations in propionic acidemia. J Hum Genet. 2006;51:992–997. doi: 10.1007/s10038-006-0068-3. - DOI - PubMed
    1. Grünert SC, Müllerleile S, De Silva L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R. Propionic acidemia: neonatal versus selective metabolic screening. J Inherit Metab Dis. 2012;35:41–49. doi: 10.1007/s10545-011-9419-0. - DOI - PubMed

LinkOut - more resources