Monday , November 29 2021

Chronicle of Nuclear Power: 35 genes that contain people for CKD



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Chronicle Nationwide Influence influences one of the ten adults worldwide

Chronicle Nationwide Influence influences one of the ten adults worldwide & nbsp | & nbspPhoto Credit: & nbspThinkstock

New Delhi: In a major forehead in the understanding of the significant under-diagnosed condition, scientists identified 35 genes identified by chronic renal disease (CKD). Chronicle of nourishment, which is almost one of the world's ten adults worldwide, is known for its strong genetic component. CKD is a long-term institution where the kidneys are occupied and can not work as they should. It often has no symptoms and can not be seen until your kidney is strongly frozen.

The signs and symptoms of chronic nuclear power in & # 39; During the day may arise abuse, lack, or loss of life. appetite, minority, shortness of breath, blood in urine, swollen knees, feet or hands, etc. failure that needs is dialysis or transplantation. The researchers believe that the new findings, which have been done, were "Generation RNA sequencing" of # 39; a nineteenth-opened one of the largest e-collections of human kidneys, can improve diagnostic tests and treatments for the worsening condition. Read – Try these 4 natural families for the removal of natural stone health

Researchers have more than 100 variants connected with CKD in large scale genetic studies. However, the biological mechanisms that threaten the genetic susceptibility to CKD, appear and remain in a clinical translation of & quot; the findings of genuine scientific study surveys gradually.

"Chronicle of Native Power is known for its strong genetic component," says lead researcher Maciej Tomaszewski, professor at the University of Manchester in England. "Our limited knowledge of its genetic mechanisms shared explicit why progress in the development of new diagnostic tests and treatments of chronic nourishment was so slow," added Tomaszewski.

The researchers hope that some of the nurses they have detected are attractive goals for the development of future diagnosis and treatment for patients with chronic nourishment.

One of the genes, mucin-1, makes a sticky protein named mucine that mucous membranes in & # 39; The nerves are, said the study. Mutations of this gene are already found in rare families with inherited nerve.

"We hope that strange prediction by genetic testing even before the development of symptoms in the future will be the first line of defense against one of the world's top brushes," said Professor Fadi Charchar from & # 39; the Federation of Australia.

"Early detection followed by treatment of renal-protecting medication or failure of medicines that damage the kidneys is the key to healthy kidneys later in life."

The findings are published in the journal Nature Communications.

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