Congenital Cystic Kidney Disease

Autosomal recessive polycystic kidney disease (ARPKD): ARPKD is the rarest case seen in polycystic kidney disease patients. This disease is transferred by a recessive gene The symptoms of the disease are noticed immediately after the birth, sometimes they don’t appear until later in childhood.

Kidneys are important organs of the body that chiefly function to remove toxins, waste and excess water out of the body through the medium of urine. Kidney diseases can be affected by both lifestyle changes and genetics. Congenital cystic kidney disease is a kidney disorder develops through a genetic mutation in the body cells. “Congenital cystic kidney disease”

Polycystic kidney disease is a congenital cystic kidney disease in which clusters of cysts develop in the lining of the kidneys. These cysts are the fluid-filled sacs that are non- cancerous and vary in sizes.

SYMPTOMS OF CONGENITAL CYSTIC KIDNEY DISEASE:

The congenital cystic kidney disease develops several noticeable symptoms such as:

Headaches
Frequent urination and blood in urine
Back pain or side pain
Hypertension / High blood pressure
Kidney stones
Enlarged abdomen due to increased kidney size
Kidney failure
Kidney or urinary tract infections “Congenital cystic kidney disease”

COMPLICATIONS OF CONGENITAL CYSTIC KIDNEY DISEASE:

The development of kidneys can affect other areas of the organ causing multiple other complications like:

Chronic high blood pressure: hypertension is the most common outcome of congenital cystic kidney disease
Kidney failure and loss of kidney functions: kidney failure is the progressed stage of congenital cystic kidney disease that hits patients after the age of 60’s
Cysts in the liver: cysts in the liver are the common instance seen in women with congenital cystic kidney disease.
A brain aneurysm
Chronic pain “Congenital cystic kidney disease”
Colon problems: Pouches in the colon may develop as a result of congenital cystic kidney disease.

REASONS BEHIND CONGENITAL CYSTIC KIDNEY DISEASE:

Genetic mutation is the prime cause of congenital cystic kidney disease. There are two major genetic defects witnessed that can cause polycystic kidney disease:

Autosomal dominant polycystic kidney disease (ADPKD): This disease is transferred by a dominant gene. No symptoms are visible until the age of 30-40 years. ADPKD is the common type seen in polycystic kidney disease patients.

HOW TO DIAGNOSE AND TREAT CONGENITAL CYSTIC KIDNEY DISEASE?

Congenital cystic kidney disease is diagnosed few different tests like CT SCAN, ULTRASOUND, and MRI. These tests reveal the actual structure of the kidneys that help in detecting the size of the cysts and the enlarged kidneys. “Congenital cystic kidney disease”

Allopathy claims that there is no cure for congenital cystic kidney disease. Once it has happened it cannot be reversed rather can be managed throughout the life. It offers symptomatic treatment of polycystic kidney disease by relieving the effects of the complications caused by the disease."Karma Ayurveda Reviews"

NATURALLY AIDING CONGENITAL CYSTIC KIDNEY DISEASE:

Unlike allopathy, Ayurveda has a completely different standpoint on this subject. It claims that all kidney disorders can be treated by using a correct line of treatment. Ayurveda employs naturally grown herbs in their medicines and offers healthy renal diets that smoothly relieves the effects of the congenital cystic kidney disease and also reverse the impairment. “Congenital cystic kidney disease”, Ayurvedic treatment measures are a permanent cure of all body ailments, without any side effects.

Karma Ayurveda, a kidney treatment hospital is the finest Ayurveda centre that works under the line of natural measures. This kidney treatment centre is proudly owned by a prominent physician Dr. Puneet Dhawan whose safe ayurvedic treatment measures have saved the lives of thousands of kidney patients without the need for dialysis.