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.
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causes, and treatments of Galactosemia I is available below.
Symptoms of Galactosemia I
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symptoms of Galactosemia I
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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
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Disease Topics Related To Galactosemia I
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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 often fails to be correctly diagnosed....read more »
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Galactosemia I: Animations
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Statistics for Galactosemia I
Galactosemia I: Broader Related Topics
Types of Galactosemia I
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