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Neonatal Bartter syndrome with unilateral multicystic dysplastic kidney disease.

作者信息

Tomimatsu Takuji, Fukuda Hirotsugu, Kanzaki Toru, Hirano Shinya, Wada Kazuko, Murata Yuji

机构信息

Department of Obstetrics and Gynecology, Osaka University Faculty of Medicine, 2-2, Yamada-oka, Suita, 565-0871, Osaka, Japan.

出版信息

Pediatr Nephrol. 2003 Apr;18(4):391-3. doi: 10.1007/s00467-002-1043-7. Epub 2003 Feb 7.

DOI:10.1007/s00467-002-1043-7
PMID:12700968
Abstract

Neonatal Bartter syndrome is characterized by antenatal presentation with polyhydramnios. In this paper, we report a case of neonatal Bartter syndrome associated with unilateral multicystic dysplastic kidney disease. To our knowledge, this is the first case report of such an association.

摘要

相似文献

1
Neonatal Bartter syndrome with unilateral multicystic dysplastic kidney disease.
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2
Diagnosis of antenatal Bartter syndrome.产前巴特综合征的诊断。
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3
[Bartter syndrome--a rare cause of severe polyhydramnios].[巴特综合征——严重羊水过多的罕见病因]
Ugeskr Laeger. 2006 Dec 11;168(50):4425-6.
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[Fetal polyuria and decrease of electrolytes in amniotic fluid as principal markers of neonatal Bartter's syndrome].[胎儿多尿及羊水电解质减少作为新生儿巴特综合征的主要标志物]
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Antenatal Bartter syndrome: a rare cause of unexplained severe polyhydramnios.产前巴特综合征：不明原因严重羊水过多的罕见病因。
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Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone.巴特综合征的产前诊断：羊水醛固酮
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9
Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone.巴特综合征的产前诊断：羊水醛固酮。
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Electrolyte composition of the amniotic fluid in Bartter syndrome.巴特综合征患者羊水的电解质成分
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本文引用的文献

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Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome.伴有醛固酮增多症和低钾性碱中毒的肾小球旁复合体增生。一种新综合征。
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Dysplastic and polycystic kidneys: diagnosis, associations and management.发育异常性和多囊性肾病：诊断、关联因素与管理
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Review article: The molecular era of bladder research. Transgenic mice as experimental tools in the study of outlet obstruction.综述文章：膀胱研究的分子时代。转基因小鼠作为出口梗阻研究中的实验工具。
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Biochemical examination of mother's urine is useful for prenatal diagnosis of Bartter syndrome.
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6
Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes.羊膜细胞基因诊断后高前列腺素E综合征的产前和产后管理。
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7
Neonatal Bartter syndrome--use of indomethacin in the newborn period and prevention of growth failure.新生儿巴特综合征——吲哚美辛在新生儿期的应用及生长发育迟缓的预防
Pediatr Nephrol. 1996 Dec;10(6):756-8. doi: 10.1007/s004670050210.
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Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.钾离子通道ROMK突变揭示的巴特综合征的遗传异质性。
Nat Genet. 1996 Oct;14(2):152-6. doi: 10.1038/ng1096-152.
9
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.巴特综合征，即伴有高钙尿症的低钾性碱中毒，由钠-钾-2氯协同转运蛋白NKCC2的突变引起。
Nat Genet. 1996 Jun;13(2):183-8. doi: 10.1038/ng0696-183.
10
Prenatal diagnosis of Bartter syndrome.巴特综合征的产前诊断。
Prenat Diagn. 1994 Oct;14(10):996-8. doi: 10.1002/pd.1970141017.