Rare variant of bartter syndrome with sensorineural deafness

Rajesh Kumar; Pankaj Kumar; Manoj Kumar

doi:10.3126/jnps.v35i3.13076

Rare variant of bartter syndrome with sensorineural deafness

Rajesh Kumar, Pankaj Kumar, Manoj Kumar

SN Medical College

Research output: Contribution to journal › Article › peer-review

Abstract

Bartter syndrome is an inherited renal tubular disorder characterized by hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia, hyper-prostaglandinism, normal blood pressure, with increased urinary loss of sodium, chloride, potassium, calcium and prostaglandins. There are five known type of Bartter syndrome, out of which type 4 and 5 are very rare. We are presenting here a case of Bartter syndrome with sensorineural hearing loss.

Original language	English
Pages (from-to)	293-294
Number of pages	2
Journal	Journal of Nepal Paediatric Society
Volume	35
Issue number	3
DOIs	https://doi.org/10.3126/jnps.v35i3.13076
State	Published - 2015
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2015, Nepal Paediatric Society (NEPAS). All rights reserved.

Keywords

Bartter syndrome
Hypokalemia
Metabolic alkalosis
Sensorineural hearing loss

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10.3126/jnps.v35i3.13076

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Rare variant of bartter syndrome with sensorineural deafness

Abstract

Bibliographical note

Keywords

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