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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

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly...read more »

Galactosemia III: Research Doctors & 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

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Galactosemia III: Broader Related Topics

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