First report of prenatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in a pregnancy at risk

C. Pérez-Cerdá, B. Merinero, A. Jiménez, M. J. García, P. Sanz, L. IJlst, R. J. Wanders, M. Ugarte

Research output: Contribution to journalComment/Letter to the editorAcademic

13 Citations (Scopus)

Abstract

Prenatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase (3-HAD) deficiency was performed in a family at risk. The diagnosis of an affected fetus was carried out by enzyme assay in cultured chorionic villus cells
Original languageEnglish
Pages (from-to)529-533
JournalPrenatal diagnosis
Volume13
Issue number6
DOIs
Publication statusPublished - 1993

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