Problem description: Condition description (time of onset, main symptoms, symptom changes, etc.): The child was born 20 days, and the doctor said that the plantar blood was screened for phenylalanine 1.5, the normal value is below 1.2, let go Re-examination, is this situation serious? Could it be the diagnosis of hyperphenylalanineemia?
Question date:2020-10-26
Patient information:Age: 20 days Gender: Female
Question analysis: Hello, if phenylalanine continues to be high, then you have to consider whether you have phenylketonuria, which is a genetic metabolic disease. Symptoms of this disease can appear in the baby from four to nine months, showing mental and physical development delays, as well as neurological manifestations. Early detection and early treatment will have a better recovery effect.
Guidelines: Generally, if there is a problem with plantar blood sampling, then venous blood needs to be drawn for reexamination. It is recommended that you take your baby to the hospital for review immediately.
Recommendations are for reference only. If the problem is serious, please go to the hospital for detailed inspection