Description of kidney inflammation Pyelonephritis is an infectious inflammatory kidney disease,usually of bacterial origin (literally is an inflammation of the renal pelvis and kidney). It may occur as an acute (a rapid onset, progress with significant symptoms) or chronic (long-lasting,…
smelling urine
The urine leaves the body with water and metabolites from protein breakdown, but also other important substances such as ions and salts. Changing the composition of urine can occur on its color,density or odor. Special smell of urine can be caused by a change of diet and neznačit any serious problem. At the odor is reflected aromatic foods like garlic or tropical fruit, powerful sweet smell of urine after having vitamin B12.
In the liver or kidneys in urine can detect metabolites, which would normally excreted ever been.Liver disease causes odor caused by sulfur amino acids. On the composition of urine is influenced by other metabolic disorders such as diabetes or diabetes. When compensation is bad urine smellacetone.
Putrid smell may have urine for bacterial infections of the lower urinary tract, especially when after a prolonged shutdown propagated bacteria produce increased amounts of smelly bacterial products.
To remove the smell of urine is necessary to keep drinking regime because concentrated urine odor intensity. Ammonia and urea are felt more strongly in the excessive consumption of meat. This should not exceed the norm, since these metabolites, proteins can accumulate in the body and cause, for example gout. If the odor of urine associated with cutting and burning urination make it harder, it’s probably a bacterial inflammation and is necessary as soon as possible to go beyond the family doctor, who probably prescribe antibiotics. The other changes in the smell of urine, if they persist even after adjusting diet and drinking it is advisable to consult, because of metabolic disorders your doctor.
Sicknesses with this symptom:
Phenylketonuria
Description phenylketonuria Phenylketonuria is an inherited disorder of metabolism of aromatic acids with a complete deficit of phenylalanine hydroxylase, the enzyme converting the amino acid phenylalanine to tyrosine, or its cofactor (cofactor is basically a “helper” enzyme), tetrahydrobiopterin (BH 4),…