Pregnancy in Inherited Hypokalemic Salt-Losing Renal Tubular Disorder

被引:22
|
作者
Mascetti, Laura
Bettinelli, Alberto
Simonetti, Giacomo D.
Tagliabue, Alessandro
Syren, Marie Lousie
Nordio, Francesco
Bianchetti, Mario G.
机构
[1] Mandic Hosp, Div Pediat, Merate, Italy
[2] Univ Bern, Bern, Switzerland
[3] Univ Milan, Dept Mother Child Sci, Milan, Italy
[4] Univ Milan, Dept Environm & Occupat Hlth, Milan, Italy
[5] Osped Maggiore Policlin, IRCCS Fdn Ca Granda, Milan, Italy
[6] Hosp Mendrisio, Div Pediat, Mendrisio, Switzerland
[7] Hosp Bellinzona, Div Pediat, Bellinzona, Switzerland
来源
OBSTETRICS AND GYNECOLOGY | 2011年 / 117卷 / 02期
关键词
MATERNAL BARTTERS-SYNDROME; METABOLIC ALKALOSIS; GITELMAN-SYNDROME; BLOOD-PRESSURE; SPIRONOLACTONE; POTASSIUM; AMILORIDE; THERAPY;
D O I
10.1097/AOG.0b013e3182075317
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: The management of inherited hypokalemia has improved and the issue of pregnancy has become important. CASES: Between 1992 and 2010, five Italian women with the clinical diagnosis of Gitelman syndrome gave birth to a total of six newborns. Pregnancy was uneventful in four women but was complicated by tiredness and tetanic seizures in the fifth woman. Drug management included potassium chloride in four cases and magnesium and amiloride in one case each. The six neonates were born at term (n=4) or near term (n=2), with a body weight that was appropriate for gestational age. The children, aged between 6 weeks and 18 years, were healthy and neurodevelopmentally and somatically normal at the last follow-up. CONCLUSION: Women with hypokalemia can become pregnant and the disorder may be managed without negative effect on the fetus. (Obstet Gynecol 2011;117:512-6) DOI: 10.1097/AOG.0b013e3182075317
引用
收藏
页码:512 / 516
页数:6
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