Can polycystic kidney give birth to a child

summary

Uncle because has been working in the coal mine, so fell the occupational disease, and got a very serious polycystic kidney disease. Now I have been cultivating at home, and then I went to the hospital for treatment. I plan to have another child. The doctor said that I recovered well under active treatment. Next, I will tell you about polycystic kidney can give birth to children

Can polycystic kidney give birth to a child

First: polycystic kidney has a certain relationship with heredity and fertility. This paper specifically introduces the question of whether polycystic kidney can give birth to children. Patients with polycystic kidney should wait until their condition is stable before they consider having a baby. Polycystic kidney disease can be divided into autosomal recessive disease (ARPKD) and autosomal dominant disease (ADPKD). The heritability of ARPKD and ADPKD was 75% and 50%, respectively.

Second, although the heritability is high, it is not uncontrollable. Experts suggest that polycystic kidney patients in the stable stage of the disease (that is, hypertension, hematuria and other indicators under control, no urinary tract infection, cyst bleeding and hydronephrosis symptoms) to consider to have a baby, not only is conducive to the recovery of the patient's condition, and according to clinical observation, at this time the heritability will be greatly reduced.

Third: polycystic kidney should be monitored regularly. Considering that the treatment of polycystic kidney is complicated in the later stage, in order to ensure the health of the baby and realize the eugenics, it is extremely necessary for women with polycystic kidney to have B-ultrasound examination on the fetus regularly during pregnancy.

matters needing attention

Polycystic kidney disease is a kind of hereditary kidney disease. It is mainly manifested as multiple cysts of different sizes in bilateral kidneys. The disease is autosomal dominant inheritance. According to its genetic law, the incidence of male and female is equal. The incidence of one parent's children is 50%. But about 40% of the patients have no family genetic history, which may be caused by their own gene mutation