Firshein S I, Hoyer L W, Lazarchick J, Forget B G, Hobbins J C, Clyne L P, Pitlick F A, Muir W A, Merkatz I R, Mahoney M J
N Engl J Med. 1979 Apr 26;300(17):937-41. doi: 10.1056/NEJM197904263001701.
Prenatal diagnosis of classic hemophilia (hemophilia A) in mid-trimester was achieved by means of immunoradiometric assays for factor VIII on fetal plasma and amniotic-fluid mixtures obtained by fetoscopy. Samples were analyzed from six male fetuses at risk for severe hemophilia and from nine control fetuses for which fetoscopy was carried out to attempt prenatal diagnosis of other genetic disorders. The factor VIII coagulant-antigen values for the control (non-hemophilic) samples were 17 to 94, and the factor VIII related-antigen concentrations were 50 to 155 U per deciliter. Three of the fetuses at risk for hemophilia had factor VIII values in the control range, and these infants were normal at birth. The other three fetuses had low concentrations of factor VIII coagulant antigen but normal concentrations of factor VIII related antigen. These values and the diagnoses of severe hemophilia were confirmed with blood from the abortuses.
通过对胎儿镜检查获取的胎儿血浆与羊水混合物进行凝血因子VIII免疫放射分析,实现了孕中期典型血友病(血友病A)的产前诊断。对6例有严重血友病风险的男性胎儿样本以及9例接受胎儿镜检查以尝试对其他遗传疾病进行产前诊断的对照胎儿样本进行了分析。对照(非血友病)样本的凝血因子VIII促凝剂抗原值为17至94,凝血因子VIII相关抗原浓度为每分升50至155单位。3例有血友病风险的胎儿其凝血因子VIII值在对照范围内,这些婴儿出生时正常。另外3例胎儿的凝血因子VIII促凝剂抗原浓度较低,但凝血因子VIII相关抗原浓度正常。这些数值以及严重血友病的诊断通过流产胎儿的血液得到了证实。