دورية أكاديمية

Unusual case of failure to thrive: Type III Bartter syndrome

التفاصيل البيبلوغرافية
العنوان: Unusual case of failure to thrive: Type III Bartter syndrome
المؤلفون: Sumit Agrawal, Krishnahari Subedi, Pankaj Ray, Ajit Rayamajhi
المصدر: Journal of Nepal Health Research Council, Vol 14, Iss 3 (2017)
بيانات النشر: Nepal Health Research Council, 2017.
سنة النشر: 2017
المجموعة: LCC:Public aspects of medicine
مصطلحات موضوعية: Public aspects of medicine, RA1-1270
الوصف: Bartter syndrome Type III is a rare autosomal recessive disorder resulting from an inherited defect in the thick ascending limb of the loop of henle of the nephrons in kidney. The typical clinical manifestations in childhood are failure to thrive and recurrent episodes of vomiting. Typical laboratory findings which help in the diagnosis are hypokalemic metabolic alkalosis, hypomagnesemia and hypercalciuria. We report a case of Type III Bartter syndrome not responding to repeated conventional treatment of failure to thrive. Keywords: Bartter syndrome; failure to thrive; hypercalciuria; hypomagnesemia; hypokalemia
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1727-5482
1999-6217
Relation: https://jnhrc.com.np/index.php/jnhrc/article/view/880; https://doaj.org/toc/1727-5482; https://doaj.org/toc/1999-6217
DOI: 10.33314/jnhrc.v14i3.880
URL الوصول: https://doaj.org/article/b2927e3808ca4b54b1174ca097accfd7
رقم الأكسشن: edsdoj.b2927e3808ca4b54b1174ca097accfd7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17275482
19996217
DOI:10.33314/jnhrc.v14i3.880