Pseudo-Bartter Syndrome in a Chinese Infant with Cystic Fibrosis Caused by c.532G ＞A Mutation in CFTR

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摘要To the Editor:We present a Chinese case of cystic fibrosis (CF) with Pseudo-Bartter syndrome (PBS) in a 6-month-old female infant.She started to have recurrent cough and wheezing after "a common cold" at 3-month-old and had been hospitalized several times for "pneumonia".She received oral antibiotics and nebulized bronchodilators which resulted in no improvement.In addition,she developed hypokalemia (2.5 mmol/L) and metabolic alkalosis.She was transferred to our hospital for ongoing care.She had an uncomplicated birth history.She was the fourth child born to consanguineous parents.Her elder brother died of severe pneumonia and bronchiectasis at 13 years of age.

作者单位 National Clinical Research Center for Respiratory Diseases, Department of Respiratory Medicine, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China ^[1]

栏目名称

Correspondence

DOI 10.4103/0366-6999.218015

发布时间 2018-01-03

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