O'Sullivan E, Monga M, Graves W
Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Texas Medical School, Houston 77030, USA.
Am J Perinatol. 1997 Jan;14(1):55-7. doi: 10.1055/s-2007-994097.
Bartter's syndrome is a rare autosomal recessive disorder characterized by hypokalemia, hyperaldosteronism, sodium wasting, normal blood pressure, hypochloremic alkalosis, and hyperplasia of the juxtaglomerular apparatus. We present a 21-year-old African-American nulliparous patient who was referred to our clinic at 9 weeks' gestation with a history of Bartter's syndrome. Her antenatal course was complicated by muscle cramps, which required increasing potassium supplementation. She developed hypomagnesemia in the third trimester of pregnancy, which necessitated magnesium therapy. She delivered an unaffected infant at term. Bartter's syndrome, although extremely rare in pregnancy, requires prompt recognition and careful management, as it may have significant maternal and neonatal implications.
巴特综合征是一种罕见的常染色体隐性疾病,其特征为低钾血症、醛固酮增多症、钠丢失、血压正常、低氯性碱中毒以及肾小球旁器增生。我们报告一名21岁未生育的非裔美国女性患者,她在妊娠9周时因巴特综合征病史转诊至我们的诊所。她的产前过程因肌肉痉挛而复杂化,这需要增加钾补充剂。她在妊娠晚期出现低镁血症,这需要进行镁治疗。她足月分娩了一名未受影响的婴儿。巴特综合征虽然在妊娠中极为罕见,但需要及时识别和谨慎管理,因为它可能对母亲和新生儿有重大影响。