Prenatal diagnosis of isovaleric acidaemia by enzyme and metabolite assay in the first and second trimesters
Prenatal Diagnosis , Volume 15 - Issue 6 p. 527- 533
Isovaleric acidaemia (IVA) is caused by a deficiency of isovaleryl CoA dehydrogenase. The diagnosis can be established biochemically by the demonstration of increased levels of isovalerylglycine (IVG) and 3-hydroxyisovaleric acid in urine and by the deficiency of incorporation of radiolabel from [14C]isovaleric acid in macromolecules in cultured fibroblasts. This paper reports a consecutive series of 24 prenatal diagnoses in pregnancies at high risk, using both methods-metabolite and indirect enzyme assay. Affected fetuses were diagnosed in four pregnancies: three in the second trimester and one recent case in the first trimester. The latter represents the first reported case of a first-trimester diagnosis of IVA by direct analysis of chorionic villi. We also report the first demonstration of strongly accumulated IVG in the amniotic fluid in the 12th week of an affected pregnancy.
|Amniotic fluid, Chorionic villi, Isovaleric acidaemia, Isovaleryglycine, Prenatal diagnosis|
|Organisation||Department of Clinical Genetics|
Kleijer, W.J, van der Kraan, M, Huijmans, J.G.M, van den Heuvel, C.M.M, & Jakobs, C. (1995). Prenatal diagnosis of isovaleric acidaemia by enzyme and metabolite assay in the first and second trimesters. Prenatal Diagnosis, 15(6), 527–533. doi:10.1002/pd.1970150605