In most cases, neonatal Bartter syndrome happens during the twenty-fourth to thirtieth week of gestation with polyhydramnios or excessive amniotic fluid. Because of this, the infant will have condition known as polyuria or excessive urination and polydipsia or excessive consumption of fluids. If the infant does not receive requisite quantities of fluids, the complications could be life-threatening. Although these symptoms begin at the first two years after birth, they are most likely diagnosed only after the child is in schooling age. Symptoms include: Growth failure - Rate of weight gain is much lower than that of other children of similar age and gender Constipation Low blood pressure Kidney stones Muscle cramping and weakness Higher urination frequencyDFDAFF
Bartter syndrome is caused due to genetic mutations during the birth of the child. The causes of Bartter syndrome are unknown yet.
Most kidney-related issues cause blood pressure, but Bartter syndrome causes low blood pressure. The above-mentioned symptoms could happen in people who take too many diuretics and laxatives. Bartter syndrome is diagnosed mainly by using blood tests and urine tests. Blood Tests Urine Test Ultrasound Scans
If you have Bartter syndrome, your nephrologist may recommend the following treatment procedures to cure you
There are no known prevention methodologies for Bartter syndrome, because the disease results from mutations of the genes.
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