What is Polycystic Kidney Disease
Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The kidneys are two organs, each about the size of a fist, located in the upper part of a person's abdomen, toward the back. The kidneys filter wastes and extra fluid from the blood to form urine. They also regulate amounts of certain vital substances in the body. When cysts form in the kidneys, they are filled with fluid. PKD cysts can profoundly enlarge the kidneys while replacing much of the normal structure, resulting in reduced kidney function and leading to kidney failure.
Polycystic Kidney Disease Causes
In some cases, a person with ADPKD has no known family history of the disease. However, it's possible that someone in the affected person's family actually did have the disease, but didn't show signs or symptoms before dying of other causes. In a smaller percentage of cases where no family history is present, ADPKD results from a spontaneous gene mutation.
Autosomal dominant PKD makes up about 90 percent of all cases of PKD. Mutations in the PKD1 and PKD2 genes cause autosomal dominant PKD. Chromosome 16 and chromosome 4 host the PKD1 and PKD2 gene respectively. Mutated PKD1 and PKD2 genes cause the production of polycystin-1 and polycystin-2 proteins which causes production of multiple cysts in the kidneys and other places in the body. Children of parents with autosomal dominant PKD have a 50 percent chance of inheriting the gene. About half of people with autosomal dominant PKD progress to kidney failure.
Polycystic Kidney Disease Symptoms
Early in the disease, patients often experience no symptoms. In fact, many people don't realize they have ADPKD because they have so few if any symptoms.
Some of the most common symptoms of polycystic kidney disease are:
frequent kidney infections
high blood pressure
back and side pains
blood in the urine
urinary tract infections
liver and pancreatic cysts
abnormal heart valves
kidney stones
aneurysms in the brain
diverticulosis
How To Treat Polycystic Kidney Disease
Micro-Chinese Medicine Osmotherapy is a new treatment method which has been studied by Kidney Disease Hospital through many years clinical experience. Through skin penetration, the micro-processing Chinese medicine will dilate the vessel, accelerate blood circulation, remove the cystic fluid quickly as well as reduce capsule pressure, inhibit the continuous secretion of wall epithelial cells, reduce the cyst fluid generation, make the cyst continue to shrink and effectively prevent the cyst from increasing, thus reducing the damage of kidney organization and achieve the purpose of treating disease.
Micro-Chinese Medicine Osmotherapy can reduce the formation of cystic fluid, alleviate the oppression of glomeruli, tubules and renal vessels, promote the circulation of the damaged kidney organization, improve the state of renal anoxia and provide a favorable environment for accelerating the repair of damaged kidneys.
Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The kidneys are two organs, each about the size of a fist, located in the upper part of a person's abdomen, toward the back. The kidneys filter wastes and extra fluid from the blood to form urine. They also regulate amounts of certain vital substances in the body. When cysts form in the kidneys, they are filled with fluid. PKD cysts can profoundly enlarge the kidneys while replacing much of the normal structure, resulting in reduced kidney function and leading to kidney failure.
Polycystic Kidney Disease Causes
In some cases, a person with ADPKD has no known family history of the disease. However, it's possible that someone in the affected person's family actually did have the disease, but didn't show signs or symptoms before dying of other causes. In a smaller percentage of cases where no family history is present, ADPKD results from a spontaneous gene mutation.
Autosomal dominant PKD makes up about 90 percent of all cases of PKD. Mutations in the PKD1 and PKD2 genes cause autosomal dominant PKD. Chromosome 16 and chromosome 4 host the PKD1 and PKD2 gene respectively. Mutated PKD1 and PKD2 genes cause the production of polycystin-1 and polycystin-2 proteins which causes production of multiple cysts in the kidneys and other places in the body. Children of parents with autosomal dominant PKD have a 50 percent chance of inheriting the gene. About half of people with autosomal dominant PKD progress to kidney failure.
Polycystic Kidney Disease Symptoms
Early in the disease, patients often experience no symptoms. In fact, many people don't realize they have ADPKD because they have so few if any symptoms.
Some of the most common symptoms of polycystic kidney disease are:
frequent kidney infections
high blood pressure
back and side pains
blood in the urine
urinary tract infections
liver and pancreatic cysts
abnormal heart valves
kidney stones
aneurysms in the brain
diverticulosis
How To Treat Polycystic Kidney Disease
Micro-Chinese Medicine Osmotherapy is a new treatment method which has been studied by Kidney Disease Hospital through many years clinical experience. Through skin penetration, the micro-processing Chinese medicine will dilate the vessel, accelerate blood circulation, remove the cystic fluid quickly as well as reduce capsule pressure, inhibit the continuous secretion of wall epithelial cells, reduce the cyst fluid generation, make the cyst continue to shrink and effectively prevent the cyst from increasing, thus reducing the damage of kidney organization and achieve the purpose of treating disease.
Micro-Chinese Medicine Osmotherapy can reduce the formation of cystic fluid, alleviate the oppression of glomeruli, tubules and renal vessels, promote the circulation of the damaged kidney organization, improve the state of renal anoxia and provide a favorable environment for accelerating the repair of damaged kidneys.
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