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首页> 外文期刊>Indian journal of nephrology >Neonatal Bartter syndrome associated with ileal atresia and cystic fibrosis
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Neonatal Bartter syndrome associated with ileal atresia and cystic fibrosis

机译:与回肠闭锁和囊性纤维化相关的新生儿Bartter综合征

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A rare case of neonatal Bartter syndrome presenting with severe hyperkalemia is reported in a preterm child born to consanguineous parents. This child also had ileal atresia, and meconium plugs were found at laparotomy. The diagnosis of cystic fibrosis was subsequently made on genetic testing. Despite full intensive care management and surgical interventions, he died of respiratory failure after 70 days. This is the first reported case of such conglomeration of pathologies in a newborn child. Second, in highlighting this case we want clinicians to be aware that a subtype of neonatal Bartter syndrome can present with initial hyperkalemia so that an erroneous diagnosis of pseudohypoaldosteronism is not made when this is seen in combination with hyperkalemia and hyperrenin hyperaldosteronism.Keywords: Cystic fibrosis, ileal atresia, neonatal bartter syndrome, pseudo-hypoaldosteronism
机译:据报道,近亲父母出生的早产儿罕见发生严重高钾血症的新生儿巴特综合征。这个孩子也有回肠闭锁,在剖腹手术中发现了胎粪栓。囊性纤维化的诊断随后通过基因检测进行。尽管进行了全面的重症监护管理和外科手术,但他在70天后死于呼吸衰竭。这是首次报道的这种病理合并症在新生儿中的案例。其次,在强调此病例时,我们希望临床医生意识到新生儿Bartter综合征的一种亚型可能伴有初始高钾血症,因此当与高钾血症和高肾素醛固酮醛固酮过多症并用时,不会对假性低醛固酮症做出错误的诊断。 ,回肠闭锁,新生儿巴特综合征,假性醛固酮增多症

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