2016年10月7日星期五

Several Symptoms of Hereditary Polycystic Kidney Disease

Polycystic Kidney Disease is caused by autosomal dominant inheritance. Cysts increase gradually with age. Epithelial cells on cystic wall secrete fluid without normal excreting channel, so cysts grow bigger gradually and cyst rupture may happen finally. Then acute abdominal infection caused by cyst rupture appears. Long-term pressure on renal parenchyma can cause renal injury inevitably, and then Renal Insufficiency, or even Uremia. Patients should pay enough attention to this disease.

Early symptoms of Polycystic Kidney Disease are backache, bellyache, and sometimes patients feel really painful. The disease attack constantly or intermittently, sometimes bellyache diffuses to back, chest, superior belly or groin. Pain can be more serious after exercise, running, and long-time sitting.
Urine abnormality: Haematuria or Albuminuria is one of early symptoms. Haematuria can present as microscopic or gross Haematuria, happening to more than 50% patients. Kidney enlargement and High Blood Pressure are more common among symptoms of PKD patients. Albuminuria can be found nearly in all cases, and most cases are mild but continuous.

Renal concentrated function decline: this symptom is mostly be found in early stage with light degree. 50%~60% patients can get Hypertension, usually appearing after renal function decline. 50% patients can get Renal Function Failure.


Firstly, in a certain time, Micro-Chinese medicine can block malignant progress of Kidney Disease which refers to blocking Renal Fibrosis. Secondly, on the basis of blocking Renal Fibrosis, Micro-Chinese Medicine can repair damaged renal inherent cells and kidney function as well as rebuild the renal normal structure. Thirdly, actively treating the other complications is helpful to achieve the effect of recovery gradually.

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