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Levels of alpha-fetoprotein during pregnancy and early infancy in normal and disease states.

机译:在正常和疾病状态下,怀孕和婴儿早期的甲胎蛋白水平。

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摘要

Alpha-fetoprotein (AFP) was 1 of the first serum protein markers to serve in the dual capacities of tumor marker and fetal defect marker, ie, an oncofetal protein, in the clinical laboratory. Although the serum-marker capacity of AFP has long been used, less is known of the fluid compartments of this oncofetal protein during fetal and perinatal development. In this review, the biologic activities of AFP are discussed in light of its presence in the various biologic fluid compartments: fetal serum, amniotic fluid, cord blood, urine, and maternal serum. AFP concentrations within the biologic fluids are considered in the context of gestational age, sex, body weight, and anatomic location. Discussion follows concerning the relationships and roles of AFP in various developmental disorders such as hypothyroidism, folate deficiencies, autoimmune disorders, acquired immunodeficiency disorder (AIDS), congenital heart defects, cystic fibrosis, preeclampsia/hypertension, and platelet aggregation disorders. Based on its presence in so many types of birth defects, malformations, and congenital anomalies, AFP can be seen to serve as a form of molecular "duct tape" during pregnancy and postnatal development.
机译:甲胎蛋白(AFP)是临床实验室中最早具有肿瘤标志物和胎儿缺陷标志物双重功能的血清蛋白标志物之一,即胎粪蛋白。尽管长期以来一直使用AFP的血清标志物功能,但在胎儿和围产期发育过程中,这种癌胚蛋白的液体区室知之甚少。在本综述中,针对AFP在各种生物液区室中的存在,对它们的生物活性进行了讨论:胎儿血清,羊水,脐带血,尿液和母体血清。在胎龄,性别,体重和解剖位置的背景下考虑生物流体中的AFP浓度。随后讨论了AFP在各种发育性疾病中的关系和作用,例如甲状腺功能减退,叶酸缺乏,自身免疫性疾病,获得性免疫缺陷性疾病(AIDS),先天性心脏缺陷,囊性纤维化,先兆子痫/高血压和血小板聚集性疾病。基于其在许多类型的先天缺陷,畸形和先天性异常中的存在,可以将AFP视为在怀孕和产后发育过程中的一种分子“导带”。

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