Koch R, Friedman E G, Wenz E, Jew K, Crowley C, Donnell G
J Inherit Metab Dis. 1986;9 Suppl 2:159-68. doi: 10.1007/BF01799700.
Pregnant women with untreated phenylketonuria (PKU) with blood phenylalanine levels greater than 1200 mumol/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 mumol/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.
患有未经治疗的苯丙酮尿症(PKU)且血液苯丙氨酸水平高于1200微摩尔/升的孕妇通常会生下患有先天性出生缺陷的后代,包括小头畸形、心脏缺陷和智力障碍。根据马布里和利维的研究,血液苯丙氨酸水平在600至1200微摩尔/升之间的高苯丙氨酸血症(HPA)女性生育后代的风险也会增加。为了进一步研究这个问题,美国国立儿童健康与人类发展研究所开展了一项为期7年的合作研究,以阐明针对这些女性的适当治疗方案。