Polycystic kidney disease other diagnostic studies: Difference between revisions
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{{Polycystic kidney disease}} | {{Polycystic kidney disease}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{MKA}} | ||
==Overview== | ==Overview== | ||
*Other diagnostic studies for polycystic kidney disease include, genetic testing, which demonstrates, frame insertions/deletions, non-canonical splice site alterations, combined missense changes. | |||
Other diagnostic studies for | |||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
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[[Category: | [[Category:Up-To-Date]] | ||
[[Category:Primary care]] | |||
[[Category:Medicine]] | |||
[[Category:Nephrology]] |
Revision as of 21:42, 5 June 2018
Polycystic kidney disease Microchapters |
Differentiating Polycystic kidney disease from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: M. Khurram Afzal, MD [2]
Overview
- Other diagnostic studies for polycystic kidney disease include, genetic testing, which demonstrates, frame insertions/deletions, non-canonical splice site alterations, combined missense changes.
Other Diagnostic Studies
- Other diagnostic studies for polycystic kidney disease include:
References
- ↑ Garcia-Gonzalez MA, Jones JG, Allen SK, Palatucci CM, Batish SD, Seltzer WK; et al. (2007). "Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease". Mol Genet Metab. 92 (1–2): 160–7. doi:10.1016/j.ymgme.2007.05.004. PMC 2085355. PMID 17574468.
- ↑ Rossetti S, Consugar MB, Chapman AB, Torres VE, Guay-Woodford LM, Grantham JJ; et al. (2007). "Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease". J Am Soc Nephrol. 18 (7): 2143–60. doi:10.1681/ASN.2006121387. PMID 17582161.