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Bartter's syndrome, type 3

Bartter's syndrome, type 3: Introduction

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. More detailed information about the symptoms, causes, and treatments of Bartter's syndrome, type 3 is available below.

Symptoms of Bartter's syndrome, type 3

Home Diagnostic Testing

Home medical testing related to Bartter's syndrome, type 3:

Wrongly Diagnosed with Bartter's syndrome, type 3?

Bartter's syndrome, type 3: Deaths

Read more about Deaths and Bartter's syndrome, type 3.

Causes of Bartter's syndrome, type 3

Read more about causes of Bartter's syndrome, type 3.

Disease Topics Related To Bartter's syndrome, type 3

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

Bartter's syndrome, type 3: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Bartter's syndrome, type 3

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Bartter's syndrome, type 3: Research Doctors & Specialists

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Hospitals & Clinics: Bartter's syndrome, type 3

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Choosing the Best Hospital: More general information, not necessarily in relation to Bartter's syndrome, type 3, on hospital performance and surgical care quality:

Bartter's syndrome, type 3: Broader Related Topics

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Videos about Bartter's syndrome, type 3

 

More information about Bartter's syndrome, type 3

  1. Bartter's syndrome, type 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Deaths
 

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