What medicine does child black acid urine syndrome take?

summary

Pediatric melanoaciduria syndrome is known as Garrod syndrome, also known as brown yellow syndrome (endogenous brown yellow disease). It is characterized by blackening of urine, melanin deposition in sclera and auricular cartilage, polyarthritis and severe pain in pubic symphysis. It is a metabolic genetic disease caused by congenital metabolic deficiency of urinary melanoxygenase. What medicine does child black acid urine syndrome take? Next, I'd like to share my views with you.

What medicine does child black acid urine syndrome take?

Once it becomes brown yellow, there is no effective treatment, so it should be treated as soon as possible. Taking vitamin C for a long time can inhibit the oxidation and polymerization of urine black acid, which may have certain significance in relieving clinical joint symptoms. Although vitamin C can reduce the excretion of urine black acid, it can not cure the disease.

If phenylalanine was ingested 200-500 mg per day, normal development might be achieved. For the treatment of joint disease is mainly appropriate rest and physical therapy, when necessary to give analgesic drugs. The patients with joint deformity can be operated as appropriate.

The color of urine can be seen as early as a few days after birth. Skin discoloration occurs in 20-30 years old, joint symptoms occur in 30-40 years old, and kidney disease occurs in 50 years old. Arthropathy can cause disability, and the survival period can be very long. The main causes of death are cardiovascular disease and uremia.

matters needing attention

Should eat the food with high protein content; It's better to eat nourishing food; Should eat warm tonic food. Mutton is a kind of hair food, but it has a good warming and tonifying effect. It is suitable for children with renal insufficiency. It has the function of nourishing kidney.