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Scheme of renal tubule and its vascular supply.
|OMIM||601678 241200 607364 602522|
Bartter syndrome is a rare inherited defect in the thick ascending limb of the loop of Henle. It is characterized by low potassium levels (hypokalemia), increased blood pH (alkalosis), and normal to low blood pressure. There are two types of Bartter syndrome: neonatal and classic. A closely associated disorder, Gitelman syndrome, is milder than both subtypes of Bartter syndrome.
In 90% of cases, neonatal Bartter syndrome is seen between 24 and 30 weeks of gestation with excess amniotic fluid (polyhydramnios). After birth, the infant is seen to urinate and drink excessively (polyuria, and polydipsia, respectively). Life-threatening dehydration may result if the infant does not receive adequate fluids. About 85% of infants dispose of excess amounts of calcium in the urine (hypercalciuria) and kidneys (nephrocalcinosis), which may lead to kidney stones. In rare occasions, the infant may progress to renal failure.
Patients with classic Bartter syndrome may have symptoms in the first two years of life, but they are usually diagnosed at school age or later. Like infants with the neonatal subtype, patients with classic Bartter syndrome also have polyuria, polydipsia, and a tendency to dehydration, but normal or just slightly increased urinary calcium excretion without the tendency to develop kidney stones. These patients also have vomiting and growth retardation. Kidney function is also normal if the disease is treated, but occasionally patients proceed to end-stage renal failure. Bartter's syndrome consists of hypokalaemia, alkalosis, normal to low blood pressures, and elevated plasma renin and aldosterone. Numerous causes of this syndrome probably exist. Diagnostic pointers include high urinary potassium and chloride despite low serum values, increased plasma renin, hyperplasia of the juxtaglomerular apparatus on renal biopsy, and careful exclusion of diuretic abuse. Excess production of renal prostaglandins is often found. Magnesium wasting may also occur.
People suffering from Bartter syndrome present symptoms that are identical to those of patients who are on loop diuretics like furosemide.
The clinical findings characteristic of Bartter syndrome are hypokalemia, metabolic alkalosis, and normal to low blood pressure. These findings may also be caused by:
- Chronic vomiting: These patients will have low urine chloride levels (Bartter's will have relatively higher urine chloride levels).
- Abuse of diuretic medications (water pills): The physician must screen urine for multiple diuretics before diagnosis is made.
- Magnesium deficiency and Calcium deficiency: These patients will also have low serum and urine magnesium and calcium
Prenatal Bartter syndrome can be associated with polyhydramnios.
Bartter syndrome is caused by mutations of genes encoding proteins that transport ions across renal cells in the thick ascending limb of the nephron.
Bartter and Gitelman syndromes can be divided into different subtypes based on the genes involved:
|Name||Bartter type||Associated gene mutations||Defect|
|neonatal Bartter's syndrome||type 1||SLC12A2 (NKCC2)||Na-K-2Cl symporter|
|neonatal Bartter's syndrome||type 2||ROMK/KCNJ1||thick ascending limb K+ channel|
|classic Bartter's syndrome||type 3||CLCNKB||Cl- channel|
|Bartter's syndrome with sensorineural deafness||type 4||BSND||Cl- channel accessory subunit|
|Bartter's syndrome associated with autosomal dominant hypocalcemia||type 5||CASR||activating mutation of the calcium-sensing receptor|
|Gitelman's syndrome||-||SLC12A3 (NCCT)||Sodium-chloride symporter|
While patients should be encouraged to include liberal amounts of sodium and potassium in their diet, potassium supplements are usually required, and spironolactone is also used to reduce potassium loss.
Nonsteroidal antiinflammatory drugs (NSAIDs) can be used as well, and are particularly helpful in patients with neonatal Bartter's syndrome.
Angiotensin-converting enzyme (ACE) inhibitors can also be used.
The limited prognostic information available suggests that early diagnosis and appropriate treatment of infants and young children with Classic Bartter Syndrome may improve growth and perhaps neurointellectual development. On the other hand, sustained hypokalemia and hyperreninemia can cause progressive tubulointerstitial nephritis, resulting in end-stage-renal disease (Kidney failure). With early treatment of the electrolyte imbalances the prognosis for patients with Classic Bartter Syndrome is good.
- Bartter and Gitelman syndromes are both characterized by hypokalemia, hypomagnesemia, normal to low blood pressure, and hypochloremic metabolic alkalosis.
However, Bartter syndrome is also characterized by high renin, high aldosterone, hypercalciuria, and an abnormal Na+-K+-2Cl- transporter in the thick ascending limb of the loop of Henle, Gitelman syndrome causes hypocalciuria and is due to an abnormal thiazide transporter in the distal segment.
Pseudo-Bartter’s syndrome is a syndrome of similar presentation as Bartter syndrome but without any of its characteristic genetic defects. Pseudo-Bartter’s syndrome has been seen in cystic fibrosis, as well as in excessive use of laxatives.
- Bartter Syndrome: Tubular and Cystic Kidney Disorders: Merck Manual Home Edition. URL accessed on 2007-12-31.
- Rodriguez-Soriano J (1998). Bartter and related syndromes: the puzzle is almost solved. Pediatr Nephrol 12 (4): 315–27.
- Bartter FC, Pronove P, Gill JR Jr, MacCardle RC (1962). Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. Am J Med 33 (6): 811–28. Reproduced in Bartter FC, Pronove P, Gill JR, MacCardle RC (1998). Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. 1962. J. Am. Soc. Nephrol. 9 (3): 516–28.
- Dane B, Yayla M, Dane C, Cetin A (2007). Prenatal diagnosis of Bartter syndrome with biochemical examination of amniotic fluid: case report. Fetal. Diagn. Ther. 22 (3): 206–8.
- Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D (2004). Bartter's and Gitelman's syndromes: from gene to clinic. Nephron Physiol 96 (3): p65–78.
- Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F (2006). Type IV Bartter syndrome: report of two new cases. Pediatr. Nephrol. 21 (6): 766–70.
- Vezzoli G, Arcidiacono T, Paloschi V, et al. (2006). Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome. J. Nephrol. 19 (4): 525–8.
- Proesmans W (2006). Threading through the mizmaze of Bartter syndrome. Pediatr. Nephrol. 21 (7): 896–902.
- Who Named It synd/2328
- Gitelman HJ, Graham JB, Welt LG (1966). A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 79: 221–35.
- Royal Brompton & Harefield Hospital > Pseudo-Bartter’s syndrome Retrieved Mars, 2011
Endocrine pathology of psychological interest (E00-35)
thyroid Hypothyroidism (Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre) - Hyperthyroidism (Graves-Basedow disease, Toxic multinodular goitre) - Thyroiditis (De Quervain's thyroiditis, Hashimoto's thyroiditis)
Genetic disorder, membrane: Channelopathy
CFTR (Cystic fibrosis, Congenital absence of the vas deferens) · CLCN1 (Thomsen disease, Myotonia congenita) · CLCN5 (Dent's disease) · CLCN7 (Osteopetrosis A2, B4 · BEST1 (Vitelliform macular dystrophy) · CLCNKB (Bartter syndrome 3)
TRPC6 (FSGS2) · TRPML1 (Mucolipidosis type IV)
GJA1 (Oculodentodigital dysplasia, Hallermann–Streiff syndrome, Hypoplastic left heart syndrome) · GJB1 (Charcot–Marie–Tooth disease X1) · GJB2 (Keratitis–ichthyosis–deafness syndrome, Ichthyosis hystrix, Bart–Pumphrey syndrome, Vohwinkel syndrome) · GJB3/GJB4 (Erythrokeratodermia variabilis, Progressive symmetric erythrokeratodermia) · GJB6 (Clouston's hidrotic ectodermal dysplasia)
AQP2 (Nephrogenic diabetes insipidus 2)
|see also ion channels|
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