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Maternal Phenylketonuria

descriptionPublicationkeyboard_double_arrow_right Article , Part of book or chapter of book 01 Jan 1986Publisher:Ovid Technologies (Wolters Kluwer Health)Journal:Obstetrical & Gynecological Survey, volume 42, pages 296-297 (issn: 0029-7828,

Authors: R, Koch; E G, Friedman; E, Wenz; K, Jew; C, Crowley; G, Donnell;

doi: 10.1097/00006254-198742050-00007 , 10.1007/bf01799700 , 10.1097/00006254-198705000-00007 , 10.1007/978-94-009-4131-1_20

pmid: 3095585

Maternal Phenylketonuria

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Abstract

AbstractPregnant women with untreated phenylketonuria (PKU) with blood phenylalanine levels greater than 1200 µmol/L usually give birth to offspring with congenital birth defects, including microcephaly, cardiac defects and mental retardation. According to Mabry and Levy, hyperphenylalaninaemic (HPA) women with blood phenylalanine levels between 600 and 1200 µmol/L also have an increased risk to their offspring. To study this problem further, the National Institute of Child Health and Human Development has established a collaborative study for 7 years to elucidate a proper treatment programme for these women.

Related Organizations

University of California System
United States

Keywords

Adult, Pregnancy Complications, Pregnancy, Phenylketonurias, Humans, Female, Diet Therapy

Impact byBIP!

	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	30
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	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 10%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Top 10%