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Galactosemia

Condition / disease reference page from the Everyone Healthy database.

Connected health information

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Condition overview

Attributes

Commonalityis rare
Incidenceis approximately 1 in 50,000 people

Linked signs and symptoms

17

Each sign/symptom opens its own page and links back to related conditions.

Linked drugs / medications

0

No linked drugs are listed yet.

Treatments, therapies and supportive options

0

Grouped by treatment type. These are educational database links, not personal treatment recommendations. Evidence labels are shown only where stored in the EH database.

No linked treatment or supportive options are listed yet.

Linked diagnostic tests and investigations

4

These are pulled from both EH diagnostic-test link tables, including the older large test-link table.

Biological and test markers

31

This visual map uses existing EH database links to show biological agents and lab markers reported as increased, decreased, or associated with this condition. These are educational relationships only; test results must be interpreted by a qualified clinician because ranges vary by lab, method, age, sex and clinical context.

Often increased

31

Often decreased

0

No markers in this group.

Other associated markers

0

No markers in this group.

Introduction / full article

Galactosemia

ID 794

Galactosemia

This is the deficiency of an enzyme that is responsible for converting galactose to glucose. Galactose is the complex form of sugar that is found in milk and some fruits. It is important that galactose is broken down to glucose so that it can be used by the body. When this breakdown is not accomplished, it can result in excessive storage of sugar in the blood, which in turn can cause damage to the liver, kidneys, and the eyes. Galactosemia can be diagnosed in newborns. This condition does not affect newborns at first, but can later on affect their appetite, growth and digestion.