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.
See full list of 26 symptoms of Galactosemia I
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