دورية أكاديمية
Unusual case of failure to thrive: Type III Bartter syndrome
العنوان: | Unusual case of failure to thrive: Type III Bartter syndrome |
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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 |
تدمد: | 17275482 19996217 |
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DOI: | 10.33314/jnhrc.v14i3.880 |