Galactosemia is a rare genetic disorder that affects an individual’s ability to metabolize galactose, a sugar found in milk and dairy products. It is typically diagnosed in infancy and requires strict dietary management. Here are key points to understand about galactosemia in children:

Genetic Cause:

  • Galactosemia is caused by mutations in genes involved in the metabolism of galactose, such as the GALT, GALE, or GALK1 genes.
  • There are different types of galactosemia, including classic galactosemia (resulting from GALT gene mutations) and variants like Duarte galactosemia.

Lack of Enzyme Activity:

  • In individuals with classic galactosemia, there is a deficiency in the enzyme galactose-1-phosphate uridylyltransferase (GALT), which is needed to break down galactose into glucose for energy.

Symptoms and Diagnosis:

  • Symptoms of galactosemia may appear shortly after birth and can include:
    • Poor feeding and growth.
    • Jaundice (yellowing of the skin and eyes).
    • Vomiting.
    • Diarrhea.
    • Liver enlargement.
  • Newborn screening tests can detect galactosemia shortly after birth.

Treatment:

  • The primary treatment for galactosemia is a strict, lifelong galactose-free diet, which requires avoiding all forms of milk and dairy products.
  • Specialized infant formula and foods that do not contain galactose are used to meet nutritional needs.
  • Compliance with the dietary restrictions is essential to prevent the buildup of toxic substances in the body.

Complications:

  • Without dietary management, galactosemia can lead to serious complications, including liver damage, cognitive impairment, and potentially life-threatening infections.

Ongoing Monitoring:

  • Children with galactosemia require regular medical monitoring to ensure that their diet is effectively preventing galactose buildup.
  • Long-term follow-up helps assess growth, development, and any potential complications.

Genetic Counseling:

  • Genetic counseling is often recommended for families affected by galactosemia to understand the risk of having another child with the condition.

Dietary Management for Life:

  • Galactosemia is a lifelong condition, and dietary management must continue throughout an individual’s life to prevent complications.
  • Adolescents and adults with galactosemia must continue to adhere to the galactose-free diet.

Prognosis:

  • With strict dietary management, many individuals with galactosemia can lead healthy lives and develop normally.
  • Early diagnosis and immediate dietary intervention are essential to prevent complications.

Galactosemia is a condition that requires lifelong dietary management, and strict adherence to the galactose-free diet is crucial for the well-being of affected children. Proper management can help prevent complications and allow individuals with galactosemia to lead healthy lives.

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