Bartter Syndrome in a Child With Solitary Functioning Kidney

نویسندگان

چکیده

Bartter Syndrome (BS) is a hereditary condition characterized by polyuria, renal salt wasting, and hypokalemic metabolic alkalosis with high serum renin aldosterone levels. Patients BS usually have symptoms in the first two years of life, but they might also be diagnosed at school age or later. Associations between congenital urinary system anomalies are extremely rare. Here we present case 4-year-old girl having solitary functioning kidney (SFK) due to right agenesis, who eventually as light clinical laboratory findings. The patient applied pediatric nephrology department complaint polyuria. Laboratory evaluation revealed hyponatremia, hypochloremia, hypokalemia alkalosis, Urine sodium, chloride, potassium excretions were increased. Sweat test was normal. CLCNKB mutation diagnosis classic negative. We assume that our another type milder mutation. Urinary accompanying very rarely reported up knowledge togetherness agenesis has not been defined literature yet.

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ژورنال

عنوان ژورنال: Türkiye çocuk hastal?klar? dergisi

سال: 2022

ISSN: ['1307-4490', '2148-3566']

DOI: https://doi.org/10.12956/tchd.940636