Duplex uterus has no obvious relationship with single kidney, the two malformations can exist separately or simultaneously, so the statement that patients with duplex uterus are prone to develop single kidney is incorrect.
Duplex uterus is a congenital malformation of uterine development. Duplex uterus is due to the fact that the bilateral paramedian tubes are not completely fused and develop into two uteruses and two cervixes, and the vaginas are also separated, and the left and right sides of the uterus each have a fallopian tube and ovary. Most often, the mother is affected by some intrinsic or extrinsic factors during embryonic development, resulting in the child having a double uterus deformity, which is not obviously related to the single kidney.
If the patient has double uterus and single kidney deformity, it is recommended to consult a doctor in time, under the guidance of the doctor, improve the relevant examination, clarify the cause of the disease and standardize the treatment.