1. Hepatocellular dysfunction |
2. Transient tryosinemia of the newborn |
3. Genetic enzyme deficiencies in tyrosine degradation |
Hepatorenal tyrosinemia (hereditary tyrosinemia type 1, HT1) |
Oculocutaneous tyrosinemia (hereditary tyrosinemia type 2, HT2) |
4-OH-phenylpyruvate dioxygenase deficiency (hereditary tyrosinemia type 3, HT3) |
4. Miscellaneous |
Scurvy |
Hyperthyroidism |
Postprandial sample |
Nitisinone therapy |
آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟