Florea Laura, Caba Lavinia, Gorduza Eusebiu Vlad
Department of Nephrology-Internal Medicine, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Department of Medical Genetics, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Front Pediatr. 2022 Jun 3;10:908655. doi: 10.3389/fped.2022.908655. eCollection 2022.
Bartter syndrome (BS) is a rare tubulopathy that causes polyuria, hypokalemia, hypochloremic metabolic alkalosis, and normotensive hyperreninemic hyperaldosteronism. It is characterized by locus, clinical, and allelic heterogeneity. Types 1-4 of BS are inherited according to an autosomal recessive pattern, while type 5, which is transient, is X linked. There are specific correlations between the clinical expression and the molecular defect, but since it is a rare disease, such studies are rare. Therapeutic interventions are different, being correlated with types of BS.
巴特综合征(BS)是一种罕见的肾小管病,可导致多尿、低钾血症、低氯性代谢性碱中毒以及血压正常的高肾素血症性醛固酮增多症。它具有位点、临床和等位基因异质性的特点。BS的1-4型按常染色体隐性模式遗传,而短暂性的5型则是X连锁的。临床表型与分子缺陷之间存在特定关联,但由于它是一种罕见疾病,此类研究较少。治疗干预措施因BS的类型而异。