Pre-eclampsia in a woman whose child suffered from lethal carnitine-acylcarnitine translocase deficiency

Authors

  • WB Geven,

    Corresponding author
    1. a Department of Pediatrics, Martini Hospital, Groningen, the Netherlandsb Laboratory for Metabolic Diseases and c Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands, d Department of Obstetrics, Martini Hospital, Groningen, the Netherlandse Department of Clinical Chemistry and Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, the Netherlandsf Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
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  • a KE Niezen-Koning,

    1. a Department of Pediatrics, Martini Hospital, Groningen, the Netherlandsb Laboratory for Metabolic Diseases and c Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands, d Department of Obstetrics, Martini Hospital, Groningen, the Netherlandse Department of Clinical Chemistry and Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, the Netherlandsf Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
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  • b A Timmer,

    1. a Department of Pediatrics, Martini Hospital, Groningen, the Netherlandsb Laboratory for Metabolic Diseases and c Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands, d Department of Obstetrics, Martini Hospital, Groningen, the Netherlandse Department of Clinical Chemistry and Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, the Netherlandsf Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
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  • c AJ Van Loon,

    1. a Department of Pediatrics, Martini Hospital, Groningen, the Netherlandsb Laboratory for Metabolic Diseases and c Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands, d Department of Obstetrics, Martini Hospital, Groningen, the Netherlandse Department of Clinical Chemistry and Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, the Netherlandsf Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
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  • d RJA Wanders,

    1. a Department of Pediatrics, Martini Hospital, Groningen, the Netherlandsb Laboratory for Metabolic Diseases and c Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands, d Department of Obstetrics, Martini Hospital, Groningen, the Netherlandse Department of Clinical Chemistry and Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, the Netherlandsf Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
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  • and e FJ Van Spronsen f

    1. a Department of Pediatrics, Martini Hospital, Groningen, the Netherlandsb Laboratory for Metabolic Diseases and c Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands, d Department of Obstetrics, Martini Hospital, Groningen, the Netherlandse Department of Clinical Chemistry and Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, the Netherlandsf Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
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Dr WB Geven, Department of Pediatrics, Martini Hospital, PO Box 30033,9700 RM Groningen, the Netherlands. Email w.b.geven@MZH.nl

No abstract is available for this article.

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