What is the Renal Oto syndrome?
Renal renal syndrome syndrome is an unusual genetic disorder where people may have a constellation of symptoms including airways, kidneys and ears. Many genes play a role in the expression of this condition and may vary in severity and nature depending on the genes that the patient inherits. Treatment focuses on providing patient support because basic genetic problems cannot be solved. Early diagnosis can provide more treatment options.
The name of this condition refers to different areas of the body involved. "Branchio" is part of the airways. In patients with renal renal syndrome, the upper airway may form incorrectly. Patients may have cysts in and on their airways and can also develop fistula, unusual openings between the airways and the neck surface. Surgery may be necessary for the treatment of these structural abnormalities.
"Oto" includes ears. The outer ear can have pits or signs of the skin and some patients of hearing or deafYou hearing. This is due to errors in the development of malformated proteins. Instead of coding for correct proteins for ears, harmful genes that cause renal renal syndrome, they cause ears to develop abnormally. These physical changes will often be clearly visible when the child is born.
Some patients also have kidney problems and explain "kidneys", although not all patients are experiencing them. In these patients, the renal renal syndrome syndrome may be associated with absent or very small kidneys, leading to renal failure and a cascading number of problems. Dialysis, transplantation and medicines can help the patient to cope with kidney problems.
As with other genetic conditions, the renal renal renal syndrome is not treatable, although gene therapy is a possibility in the future. Gene therapy could potentially allow doctors to turn off the harmaLly genes that allow healthy genes to express during embryonic development so that people do not develop physical problems due to the genes they carry.
patients may have a renal syndrome branch independently or in connection with another genetic disorder. Prenatal testing can often detect the presence of problems. This condition is dominant, which means that patients must only inherit one set of participating genes. People with genetic disorders who fear that they pass them on to children may encounter genetic advisors to discuss the risks and their possibilities. It is possible that a child may inherit a less serious form of disorder.