Discuss the genetic probability of galactosemia and its impact on parenting.

In response to the discovery of elevated levels of galactose, galactitol, and galactosamine during a urine screening at 4 months, seeking recommendations for subsequent treatment and examinations.

Can my baby eat formula without lactose if diagnosed with galactosemia?

For patients with galactosemia, how often should follow-up visits be scheduled and how to manage the intake of galactose in the diet to improve prognosis.

This article provides information about medication treatment for galactosemia.

The treatment for galactosemia usually involves dietary control to avoid the intake of foods containing lactose. This includes avoiding breast milk, cow’s milk, and other dairy products and animal organs. For infants, soy milk can be considered as an alternative. During the treatment process, regular monitoring of blood levels of galactose and galactose-1-phosphate is necessary. It should be noted that this disease cannot be completely cured, but it can be managed through dietary control.

Neonatal galactosemia is a toxic clinical metabolic syndrome characterized by elevated blood galactose levels. Treatment involves intravenous administration of glucose and fresh plasma, with attention to electrolyte supplementation.