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
See full list of 26
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
Read more about Deaths and Galactosemia I.
Galactosemia I: Complications
Review possible medical complications related to Galactosemia I:
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 often fails to be...read more »
Read more about Misdiagnosis and Galactosemia I
Galactosemia I: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Galactosemia I: Animations
More Galactosemia I animations & videos
Statistics for Galactosemia I
Galactosemia I: Broader Related Topics
Types of Galactosemia I
User Interactive Forums
Read about other experiences, ask a question about Galactosemia I, or answer someone else's question, on our message boards:
Contents for Galactosemia I:
» Next page: What is Galactosemia I?
Medical Tools & Articles:
Tools & Services:
Forums & Message Boards
- Ask or answer a question at the Boards: