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In This Topic
Kidney and Urinary Tract Disorders
Tubular and Cystic Kidney Disorders
Bartter Syndrome
Symptoms and Diagnosis
Treatment
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Chapters in Kidney and Urinary Tract Disorders
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  • Diagnosis of Kidney and Urinary Tract Disorders
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Topics in Tubular and Cystic Kidney Disorders
  • Introduction
  • Renal Tubular Acidosis (RTA)
  • Renal Glucosuria
  • Nephrogenic Diabetes Insipidus
  • Cystinuria
  • Fanconi Syndrome
  • Hypophosphatemic Rickets
  • Hartnup Disease
  • Bartter Syndrome
  • Liddle Syndrome
  • Polycystic Kidney Disease (PKD)
  • Nephronophthisis–Medullary Cystic Disease Complex
  • Medullary Sponge Kidney
 
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Bartter Syndrome

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In Bartter syndrome, the kidneys excrete excessive amounts of electrolytes (potassium, sodium, and chloride), resulting in electrolyte abnormalities in the blood.

Bartter syndrome is usually hereditary and is caused by a recessive gene. Thus, a person with the disorder has inherited two recessive genes for the disorder, one from each parent. In affected people, the kidneys excrete excessive amounts of sodium, chloride, and potassium. The loss of sodium and chloride leads to excessive urine production and thus mild dehydration, which causes the body to produce more renin and aldosterone. The increase in aldosterone increases potassium and acid secretion in the kidneys, leading to low blood potassium (hypokalemia) and loss of acids in the blood that causes blood pH to be alkaline (metabolic alkalosis–see Acid-Base Balance: Alkalosis).

Symptoms and Diagnosis

Children with Bartter syndrome grow slowly and appear malnourished. They may have muscle weakness and excessive thirst, may produce large amounts of urine, and may be mentally retarded. The loss of sodium and chloride leads to chronic mild dehydration. Abnormally low blood pressure (hypotension) may occur.

The diagnosis of Bartter syndrome in young children is based on a physical examination and on the characteristic abnormalities of electrolytes in blood and urine. Abnormal results are confirmed by finding high levels of certain hormones (renin, aldosterone) on blood tests. However, similar findings may occur when children with certain eating disorders, such as bulimia nervosa, self-induce vomiting and misuse diuretics.

Treatment

Many of the consequences of Bartter syndrome can be prevented by taking potassium supplements and a drug that reduces excretion of potassium into the urine, such as spironolactoneSome Trade Names
ALDACTONE
(which also blocks the action of aldosterone), triamtereneSome Trade Names
DYRENIUM
, amiloride, angiotensin-converting enzyme (ACE) inhibitors, or nonsteroidal anti-inflammatory drugs (NSAIDs), such as indomethacinSome Trade Names
INDOCIN
. Drinking adequate amounts of fluids is necessary to compensate for the excessive fluid losses.

Last full review/revision December 2006 by Peter C. Brazy, MD

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Pronunciations

aldosterone

alkalosis

angiotensin

electrolytes

hypokalemia

indomethacin

metabolic alkalosis

spironolactone

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