Question
Today is my baby’s 23rd day. The hospital called today to say that the baby has high levels of galactose, which is genetic galactosemia. However, the baby has been breastfed normally, sometimes consuming up to 100 milliliters, and has become visibly chubby. There is no jaundice, vomiting, or cataracts, and bowel movements are normal. The baby does not cry when hungry or after a bowel movement. If the baby really has galactosemia, will it develop normally in the future?
Answer
Case Analysis: Your baby may be a patient with galactosemia, a genetic disorder that causes the baby to be unable to metabolize lactose, leading to a series of symptoms. Currently, the baby’s symptoms are mild, possibly because timely discovery and appropriate dietary measures have been taken. Guidance: To ensure your baby’s healthy growth, it is recommended that you take your baby to the hospital for further diagnosis and treatment. In terms of diet, avoid feeding your baby foods containing lactose and switch to special formula milk or other suitable foods for galactosemic patients. Additionally, regular monitoring of your baby’s nutritional status and growth development is necessary to adjust dietary plans in a timely manner. Under the guidance of a doctor, your baby should be able to develop normally.