Polycystic kidney disease (ADPKD) name autosomal dominant polycystic kidney disease. The disease found in two age groups, adult polycystic kidney disease is a dominant genetic diseases, is caused chronic renal failure, the Common uremic one of the reasons for the abnormal growth of cysts filled with cortical and medullary quality, ranging from a hybrid of the normal kidney tissue of the organization to kidney, renal section showed pale yellow capsule containing colloidal liquid, internal bleeding may show red or brown when cysts grow to a certain stage renal capsule connected with the small hyperplasia due to pipeline and plug the cyst fluid can not be excluded, is gradually increasing. cyst epithelial lining single kidney cyst oppression, tubular atrophy and lead to sclerosis, glomerular disappeared, impaired renal function. When you abnormal growth of the cyst was covered with your kidneys, normal renal tissue will lose its function, resulting in kidney failure, due to normal renal function is to eliminate the body's waste, when the normal growth of abnormal kidney was the size of the countless earned from the time of the cyst, normal kidneys can not remove the body of waste caused by chronic renal failure and uremia development. Polycystic kidney disease cyst size, it can be from an egg the size of the ball to the size of the same, the symptoms started in 40 - 70-year-old but there are also more than 70 years the incidence, not only violations of kidney cyst, at the same time it can be violated liver, and pancreas, polycystic kidney disease not completely effective treatment.
Infantile polycystic kidney disease: stealth genetic chromosome are often are accompanied by liver disease, although mainly seen in children, but may also occur in adults, with increased renal, and maintain renal appearance. Smooth surface, but the points of the fetus more obvious, kidney honeycomb-like cut surface, a small capsule, liver portal district expansion, more typical connective tissue around the side of birth renal or kidney area increased, due at the time of birth by the mother's placenta dialysis, blood urea nitrogen, and other normal, but after a few days after birth, such as urea nitrogen into sexual increased, the general died in February, some babies survive to the age of 10, two more than the lack of a word effects therapy, Chinese medicine Some cases of this disease control development, and narrow the cyst improve renal function and alleviate symptoms corresponding treatment efficacy.
Infantile polycystic kidney disease: stealth genetic chromosome are often are accompanied by liver disease, although mainly seen in children, but may also occur in adults, with increased renal, and maintain renal appearance. Smooth surface, but the points of the fetus more obvious, kidney honeycomb-like cut surface, a small capsule, liver portal district expansion, more typical connective tissue around the side of birth renal or kidney area increased, due at the time of birth by the mother's placenta dialysis, blood urea nitrogen, and other normal, but after a few days after birth, such as urea nitrogen into sexual increased, the general died in February, some babies survive to the age of 10, two more than the lack of a word effects therapy, Chinese medicine Some cases of this disease control development, and narrow the cyst improve renal function and alleviate symptoms corresponding treatment efficacy.
