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Galactosemia I

Galactosemia I: Introduction

Galactosemia I: A rare inherited disorder where deficiency of a particular enzyme (galactose-1-phosphate uridyl transferase) prevents the metabolism of galactose which is a sugar component of milk. Ranges from milk intolerance in mild cases to death in severe untreated cases. More detailed information about the symptoms, causes, and treatments of Galactosemia I is available below.

Symptoms of Galactosemia I

Home Diagnostic Testing

Home medical testing related to Galactosemia I:

Wrongly Diagnosed with Galactosemia I?

Galactosemia I: Related Patient Stories

Galactosemia I: Deaths

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Galactosemia I: Complications

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Causes of Galactosemia I

Read more about causes of Galactosemia I.

Disease Topics Related To Galactosemia I

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

Misdiagnosis and Galactosemia I

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

Galactosemia I: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Galactosemia I: Animations

Statistics for Galactosemia I

Galactosemia I: Broader Related Topics

User Interactive Forums

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