1. Foods to avoidAvoid foods that trigger various inflammatory conditions, metabolic disorder glucose problems and triglycerides.Including the production of pro...
1. Time preparation: Blood is usually collected within 72 hours after birth, but if there is a delay due to premature infants being observed in an incubator or...
(1) Neonatal screeningAfter 3 days of feeding, blood is collected from the amino acid disorder ends of the feet and then collected on thick recycled filter pape...
Genetic metabolic diseases are caused by genetic defects in the biosynthesis of certain enzymes, inherited metabolic disorders receptors, carriers and membrane ...
Phenylketonuria is an inherited metabolic disorder mainly caused by a deficiency of the enzyme phenylalanine hydrogenase in the liver. Generally speaking, if ch...
The most obvious symptom is that the baby always has a strange odor, pku guidelines also known as mouse urine odor. There are also the following symptoms.1. Slo...
After treatment, patients on a low phenylalanine diet need to have their blood phenylalanine pku treatment monitored to keep it within the ideal range for their...
Phenylketonuria is a disorder of pku handbook amino acid metabolism. The main reason is that a series of management functions are abnormal due to accumulation o...
1、 For patients with phenylketonuria, we should first choose maternal pku the scheme of dietary treatment and how to carry out dietary treatment1. Why do you ne...
