Alberola TM, Bautista-Llacer R, Vendrell X, Garcia-Mengual E, Pardo M, et al. Case report: birth of healthy twins after preimplantation genetic diagnosis of propionic academia. J Assist Reprod Genet 2011;28:211–6.Google Scholar
Chapman KA, Summar ML. Propionic acidemia consensus conference summary. Mol Genet Metab 2012;105:3–4.Google Scholar
Van Calcar SC, Harding CO, Davidson SR, Barness LA, Wolff JA. Case reports of successful pregnancy in women with maple syrup urine disease and propioni cacidemia. Am J Med Genet 1992:44;641–6.Google Scholar
Langendonk JG, Roos JC, Angus L, Williams M, Karstens FP, et al. Aseries of pregnancies in women with inherited metabolic disease. J Inherit Metab Dis 2012;35:419–24.Google Scholar
Raval DB, Merideth M, Sloan JL, Braverman NE, Conway RL, et al. Methylmalonic academia (MMA) in pregnancy: a case series and literature review. J Inherit Metab Dis 2015;38:839–46.Google Scholar
Cordero DR, Baker J, Dorinzi D, Toffle R. Ornithine transcarbamylase deficiency in pregnancy. J Inherit Metab Dis 2005;28:237–40.Google Scholar
Lamb S, Yi Ling Aye C, Murphy E, Mackillop L. Multidisciplinary management of ornithine transcarbamylase (OTC) deficiency in pregnancy: essential to prevent hyperammonemic complications. BMJ Case Reports 2013; doi: 10.1136/bcr-2012-007416.CrossrefGoogle Scholar
About the article
Published Online: 2016-04-18
Published in Print: 2016-07-01
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.