Polycystic Kidney Disease (PKD) belongs to a kind of hereditary disease.
According the Genetics, PKD can be categorized as autosomal dominant PKD and
recessive PKD. And autosomal dominant PKD is more universal amid patients.
ADPKD belongs to autosomal dominate inheritance with characteristic of
familial aggregation. Both male and female can get this disease with equal
possibility. This disease can also inherit for generations.
ADPKD is also known as adult PKD, which is very common. With the gradual
penetration to this disease, prognosis for this disease is improved
apparently.
ARPKD belongs to autosomal recessive inheritance, which is also known as
fetus PKD. Fetus’ parents rarely have the same disease history. This type is
really seldom seen among PKD patients, and most of sick children die soon after
their birth. Only very few of them who suffer from lighter illness condition can
survive till to childhood, or even adulthood.
Micro-Chinese Medicine Osmotherapy can treat PKD effectively through the
methods of activating blood, removing blood stasis in channels and eliminating
toxin in body. Active substances of Chinese Medicine can protect remained
healthy nephron and recover injured renal cells after they entering into renal
lesion. It can treat PKD effectively with no operation and no side effect.
