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Galactosemia III

Galactosemia III: Introduction

Galactosemia III: A rare inherited disorder where deficiency of a particular enzyme (UDP-Galactose-4-epimerase) prevents the metabolism of galactose which is a sugar component of milk. The condition may vary from mild to severe. More detailed information about the symptoms, causes, and treatments of Galactosemia III is available below.

Symptoms of Galactosemia III

Home Diagnostic Testing

Home medical testing related to Galactosemia III:

Wrongly Diagnosed with Galactosemia III?

Galactosemia III: Related Patient Stories

Galactosemia III: Deaths

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Galactosemia III: Complications

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Causes of Galactosemia III

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Disease Topics Related To Galactosemia III

Research the causes of these diseases that are similar to, or related to, Galactosemia III:

Misdiagnosis and Galactosemia III

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Galactosemia III: Research Doctors & Specialists

Research related physicians and medical specialists:

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Evidence Based Medicine Research for Galactosemia III

Medical research articles related to Galactosemia III include:

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Galactosemia III: Animations

Research about Galactosemia III

Visit our research pages for current research about Galactosemia III treatments.

Galactosemia III: Broader Related Topics

User Interactive Forums

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