Polycystic kidney common clinical manifestations

Polycystic kidney disease is a genetic disease. According to the genetic characteristics, divided into autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive hereditary polycystic kidney disease (ARPKD) two categories. Autosomal dominant hereditary polycystic kidney common. ADPKD is autosomal dominant inheritance, which is characterized by a family clustering, both men and women can be the incidence of gender equality of the same opportunities for several generations can occur in patients. So what is the common clinical manifestations of polycystic kidney disease?

Should I Be Concerned about Asymptomatic PKD

Autosomal dominant polycystic kidney disease: clinical manifestations are divided into two categories of kidney and kidney.
◆ kidney performance varied, due to the growth and increase of renal cysts.
1, waist, abdominal pain is the most common, manifested as the Ministry of the Ministry, waist or abdominal pain.
2, urine abnormalities mainly manifested as hematuria or proteinuria, one of the symptoms for the earlier.
3, renal hypopnea performance for polyuria and nocturia, but less severe.
4, 50% to 60% of patients with hypertension in the course of treatment of high blood pressure.
5, renal dysfunction about 50% of patients with renal failure. With age, the incidence increased.

Symptoms of Polycystic Kidney Disease(PKD)

◆ renal manifestations: ADPKD for systemic diseases, in addition to the kidney, still involving other organs, liver cysts are the most common, about 50% of the total, and with age and increased, the number and size of the capsule gradually increased. Some patients may have fibrosis in the hilar region. But rare liver damage. Women are easily involved. A small number of patients may have abdominal pain and dyspnea and other giant hepatomegaly symptoms. Occasional liver cyst infection. Aneurysms are also important for renal manifestations. Other manifestations of the kidney are: heart valve disease; esophageal hiatal hernia, intestinal diverticulum inguinal hernia and so on.

Treatment for Polycystic Kidney Disease(PKD)

Autosomal recessive polycystic kidney: is a rare disease. 75% of children died within a few hours to several days postpartum. The survival rate of patients in the neonatal period was 50% ~ 80%. Often with liver disease. The pathogenesis of this disease is unknown, recently found abnormal gene located in the No. 6 chromosome.
Neonatal and perinatal symptoms of the main manifestations of the kidneys, infants or childhood symptoms of liver-based performance, large and adult patients rare.

PKD Treatment: Micro-Chinese Medicine Osmotherapy

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