What are the symptoms of cerebral hepatorenal syndrome?

summary

There is no definite answer to the cause of the disease. Some scientists believe that the brain liver kidney syndrome is caused by placental iron transport dysfunction. Brain liver kidney syndrome is a serious congenital disease, patients are generally born with alcohol, and generally 3-6 months patients may die, there is no effective method to treat brain liver kidney syndrome, the hospital will generally take supportive treatment. Let's take a look at the following.

What are the symptoms of cerebral hepatorenal syndrome?

First, the symptoms of brain liver kidney syndrome are very obvious. First, the patient's face will appear distortion, different from ordinary people, ears will grow deformity, forehead bulge, eyes will appear swelling, accompanied by cataract. After the patient was born, the head deformity is likely to suffer from brain liver kidney syndrome.

Second: the patient's body shape is abnormal, the body will also appear lesions. Patients with cerebral hepatorenal syndrome will suffer from nervous body weakness after birth, the whole body locked together, convulsions, often unconscious body spasms. Patients have these phenomena, it is best to ask the attending doctor in time for treatment.

Third: Patients with brain, liver and kidney syndrome can only survive for 3-6 months. During this period, the growth of patients is slower than that of normal people, dysplasia, examination also found that the liver becomes larger, cartilage calcification occurs, and there will be proteinuria and hematuria on weekdays. Brain, liver and kidney syndrome is a serious congenital disease.

matters needing attention

Because the brain liver kidney syndrome is a congenital chromosomal disease, the current medical technology has no effective preventive measures. Cerebro hepatorenal syndrome can only use liquid and semi liquid food, try not to eat food that is not easy to chew.