Sljapić N, Ancić V, Suvaković D, Gudelj S
Jugosl Ginekol Opstet. 1978 May-Aug;18(3-4):321-4.
The authors describe a case of successful pregnancy in a patent with hereditary enymopenic methemoglobinemia. The course of pregnancy was followed up by the use of ultrasound and the control of CTG, estriol, and pregnanediol. No signs of the intrauterine fetal threat were noticed. The methemoglobin value in the mother's blood ranged from 6.4% at the beginning of pregnancy to 32% at delivery, going down to 2.2% on the third postpartal day. Its reduction was increased by 2.0 to 3.0 g of C vitamin a day throughout all the time of pregnancy. The use of drugs with reduction properties is contraindicated. Genetic analysis of both parents is imperative, because a homozygote newborn could suffer from convulsions. Under conditions of present-day perinatal supervision and adequate therapy, hereditary enzymopenic methemoglobinemia is no contraindication for the performance of the reproductive function.
作者描述了一例患有遗传性酶缺乏性高铁血红蛋白血症的患者成功怀孕的病例。通过超声检查以及监测宫缩图、雌三醇和孕二醇对孕期进行了跟踪。未发现宫内胎儿有受威胁的迹象。母亲血液中的高铁血红蛋白值从怀孕初期的6.4%升至分娩时的32%,产后第三天降至2.2%。在整个孕期,每天额外补充2.0至3.0克维生素C可加速其降低。禁用具有还原特性的药物。必须对父母双方进行基因分析,因为纯合子新生儿可能会惊厥。在当今围产期监护和适当治疗的条件下,遗传性酶缺乏性高铁血红蛋白血症并非生殖功能的禁忌证。