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Genetic Diseases of the Kidney
Author(s) -
John W. Foreman
Publication year - 2015
Publication title -
the open urology and nephrology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.106
H-Index - 6
ISSN - 1874-303X
DOI - 10.2174/1874303x015080100136
Subject(s) - disease , medicine , genetic testing , prenatal diagnosis , mutation , renal biopsy , bioinformatics , kidney , identification (biology) , gene mutation , intensive care medicine , fetus , pathology , gene , genetics , pregnancy , biology , botany
The number of genes associated with renal disease is increasing every day and this has led to a clearer understanding of the pathophysiology of renal disease in many disorders. It is also appreciated now that a genetic mutation(s) underlie many renal syndromes. Genetic testing may also offer the possibility to diagnose some renal diseases without the need for a renal biopsy. It also allows the prenatal diagnosis of certain renal diseases in at risk fetuses or identification of potential renal disease before it has become manifest. Finally, identification of a specific gene mutation holds the possibility of correction though gene therapy in the future. It is increasingly clear that many renal disorders in pediatrics are a consequence of genetic mutations. In the future, genetic testing will become as easy and as common as ordering a serum creatinine today.

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