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Kelley-Seegmiller syndrome

Kelley-Seegmiller syndrome: Introduction

Kelley-Seegmiller syndrome: A rare genetic disorder characterized by the formation of stones in the urinary tract, early-onset gout and mild neurological symptoms. It is caused by a partial deficiency of hypoxanyhine-guanine phosphoribosyl transferase. More detailed information about the symptoms, causes, and treatments of Kelley-Seegmiller syndrome is available below.

Symptoms of Kelley-Seegmiller syndrome

Home Diagnostic Testing

Home medical testing related to Kelley-Seegmiller syndrome:

Wrongly Diagnosed with Kelley-Seegmiller syndrome?

Kelley-Seegmiller syndrome: Complications

Read more about complications of Kelley-Seegmiller syndrome.

Causes of Kelley-Seegmiller syndrome

Read more about causes of Kelley-Seegmiller syndrome.

Less Common Symptoms of Kelley-Seegmiller syndrome

Kelley-Seegmiller syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Kelley-Seegmiller syndrome

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Kelley-Seegmiller syndrome: Research Doctors & Specialists

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Evidence Based Medicine Research for Kelley-Seegmiller syndrome

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Research about Kelley-Seegmiller syndrome

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Kelley-Seegmiller syndrome: Broader Related Topics

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Videos about Kelley-Seegmiller syndrome

 

More information about Kelley-Seegmiller syndrome

  1. Kelley-Seegmiller syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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