How old can hereditary polycystic kidney be detected

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A friend of mine is 25 years old. He had an examination a few days ago. I don't know when he got hereditary polycystic kidney disease. Now I have been treated in the hospital, and now my condition has been controlled to a certain extent. For the problem of how old can I find out hereditary polycystic kidney disease, let me tell you.

How old can hereditary polycystic kidney be detected

First, ADPKD patients have a positive family history, and the proportion in ordinary patients is 14% L_ 41。 In 8 patients with hypertensive intracerebral hemorrhage, hypertension was not well controlled, which indicates that ADPKD complicated with intracranial hemorrhage is not only caused by intracranial aneurysm, and strict control of blood pressure is also very important. However, some patients with ADPKD and SAH have normal blood pressure, suggesting that hypertension is not necessarily a necessary factor for the development of aneurysms in ADPKD patients.

Second, the pathological changes of cerebral vessels in Alport syndrome include occlusion of anterior and middle cerebral arteries and stenosis of carotid artery lumen. The mechanism of vascular lesions is related to abnormal expression of collagen IV in cerebral vascular basement membrane.

Third: what is hereditary polycystic kidney? Polycystic kidney is a hereditary disease. According to the genetic characteristics, it can be divided into autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (AR PKD). Autosomal dominant polycystic kidney disease is common. ADPKD is autosomal dominant inheritance, which is characterized by familial aggregation. Both men and women have the same chance of being affected, and patients can appear in successive generations.

matters needing attention

Autosomal dominant polycystic kidney disease, also known as adult polycystic kidney disease, is a common polycystic kidney disease. The prognosis of the disease has been improved because of the deeper understanding of the disease. ARPKD is autosomal recessive inheritance. Almost none of the parents had the same medical history. Autosomal recessive polycystic kidney, also known as infantile polycystic kidney, is a rare type of polycystic kidney. They often die shortly after birth, and only a few of the lighter types can survive into childhood or even adulthood.