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What is Bartter's syndrome, type 3?

What is Bartter's syndrome, type 3?

  • Bartter's syndrome, type 3: A rare condition characterized by an electrolyte imbalance caused by mutations of the chloride channel gene (ClCNKb). It differs from Bartter's syndrome type I and type II in the absence of nephrocalcinosis. The severity of the condition is greatly variable.

Bartter's syndrome, type 3: Introduction

Types of Bartter's syndrome, type 3:

Broader types of Bartter's syndrome, type 3:

What causes Bartter's syndrome, type 3?

Causes of Bartter's syndrome, type 3: see causes of Bartter's syndrome, type 3

What are the symptoms of Bartter's syndrome, type 3?

Symptoms of Bartter's syndrome, type 3: see symptoms of Bartter's syndrome, type 3

Can anyone else get Bartter's syndrome, type 3?

More information: see contagiousness of Bartter's syndrome, type 3
Inheritance: see inheritance of Bartter's syndrome, type 3

Bartter's syndrome, type 3: Testing

Diagnostic testing: see tests for Bartter's syndrome, type 3.

Misdiagnosis: see misdiagnosis and Bartter's syndrome, type 3.

How is it treated?

Doctors and Medical Specialists for Bartter's syndrome, type 3: Medical Geneticist ; see also doctors and medical specialists for Bartter's syndrome, type 3.
Treatments for Bartter's syndrome, type 3: see treatments for Bartter's syndrome, type 3

Name and Aliases of Bartter's syndrome, type 3

Main name of condition: Bartter's syndrome, type 3

Other names or spellings for Bartter's syndrome, type 3:

Bartter syndrome, type 3

Bartter's syndrome, type 3: Related Conditions

Research the causes of these diseases that are similar to, or related to, Bartter's syndrome, type 3:

  • Autosomal recessive disorder
  • Secondary hyperaldosteronism
  • Impaired salt reabsorption
  • Hypokalemic alkalosis
 

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