In this article a 3 mounts old boy who diagnosed cystic fibrosis presenting as a pseudo-Bartter's syndrome was evaluated.
📌 3 Key Takeaways
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Objective & Hypothesis:Bartter syndrome are characterized by normal blood pressure, hypokalemia, metabolic alkalosis, prostaglandinuria, hyperreninemia and hyperaldosteronism and defined as a family of inherited recessive autosomal tubulopathies.
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Key Findings & Data:Pseudo-Bartter's syndrome may produce a hypokalemic metabolic alkalosis without primary renal disease.
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Conclusion & Impact:In this article a 3 mounts old boy who diagnosed cystic fibrosis presenting as a pseudo-Bartter's syndrome was evaluated.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Bartter syndrome are characterized by normal blood pressure, hypokalemia, metabolic alkalosis, prostaglandinuria, hyperreninemia and hyperaldosteronism and defined as a family of inherited recessive autosomal tubulopathies. Pseudo-Bartter's syndrome may produce a hypokalemic metabolic alkalosis without primary renal disease. The underlying illnesses are primary hyperaldosteronism, Cushing syndrome, hypertrophic pyloric stenosis, cystic fibrosis and some drogs. In this article a 3 mounts old boy who diagnosed cystic fibrosis presenting as a pseudo-Bartter's syndrome was evaluated.
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Cite This Article
DURSUN, F., DÖNMEZ, M., ERGÜVEN, M., SAĞLAM, Ö. N., FEDAKAR, A. (2022). Cystic fibrosis presenting as a Pseudo-Bartter syndrome. Göztepe Tıp Dergisi, Cilt: 18 - Sayı: 4, 243–244. https://ajindex.com/articles/526496
Sauter R, Will M, Helwig H: Severe Hyponatremia as diagnostic symptom of cystic fibrosis. Clin Pediatr 209(6):361-3, 1997
Yu HR, Huang SC, Hsieh CS: Infantile hypertrophic pyloric stenosis presenting as pseudo-Bartter's syndrome and seisures: report of one cases. Chung Hua Min Kuo Hsiao Erh Ko I Hsueh Hui Tsa Chih 39(3):195-7, 1998.