It’s quite common for newborns to be fussy during feeding, but if this issue persists, it’s important to be vigilant.

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

Galactosemia is a metabolic disorder in infants caused by a deficiency of the enzyme needed to break down lactose, leading to an increase in galactose levels in the blood.

If a child is suffering from galactosemia, the mother should immediately take the child to the doctor, avoid self-medicating, and pay close attention to the child’s condition to help them receive timely treatment.

Precautions for patients with galactosemia, as well as how to help them deal with issues such as hypertension, dizziness, and loss of appetite.

How to treat galactosemia? Information on treatment methods and potential complications

Patients with galactosemia should seek medical attention promptly, avoid misconceptions, and receive symptomatic treatment.

Amniocentesis primarily checks for fetal karyotype analysis, chromosomal genetic disease diagnosis, and the diagnosis of genetic and metabolic diseases, which is a necessary examination for elderly pregnant women.

If a child exhibits symptoms such as jaundice, loss of appetite, vomiting, and digestive problems with pale yellow or grayish stools, they should seek medical attention immediately to check for galactosemia and avoid self-administering unknown medications.

Galactosemia and lactose intolerance are two distinct diseases, the former being caused by a congenital genetic defect, and the latter being Acquired intolerance.