Horseshoe kidney risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
There are no particular gene discovered yet which are directly related to horseshoe kidney but it has been seen associated with other genetic disorders such as Turner syndrome and Edwards syndrome, further suggesting that it is linked to some genes. | There are no particular gene discovered yet which are directly related to horseshoe kidney but it has been seen associated with other genetic disorders such as [[Turner syndrome]] and [[Edwards syndrome]], further suggesting that it is linked to some genes. | ||
==Risk Factors== | ==Risk Factors== | ||
There are no | *There are no particular gene discovered yet which are directly related to horseshoe kidney but it has been seen associated with other genetic disorders such as [[Turner syndrome]] and [[Edwards syndrome]], further suggesting that it is linked to some genes.<ref name="KletaBrämswig2000">{{cite journal|last1=Kleta|first1=Robert|last2=Brämswig|first2=Jürgen H.|title=Horseshoe kidney and Turner syndrome|journal=Nephrology Dialysis Transplantation|volume=15|issue=7|year=2000|pages=1094–1094|issn=1460-2385|doi=10.1093/ndt/15.7.1094-b}}</ref> | ||
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==References== | ==References== | ||
Latest revision as of 20:20, 23 January 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
There are no particular gene discovered yet which are directly related to horseshoe kidney but it has been seen associated with other genetic disorders such as Turner syndrome and Edwards syndrome, further suggesting that it is linked to some genes.
Risk Factors
- There are no particular gene discovered yet which are directly related to horseshoe kidney but it has been seen associated with other genetic disorders such as Turner syndrome and Edwards syndrome, further suggesting that it is linked to some genes.[1]
References
- ↑ Kleta, Robert; Brämswig, Jürgen H. (2000). "Horseshoe kidney and Turner syndrome". Nephrology Dialysis Transplantation. 15 (7): 1094–1094. doi:10.1093/ndt/15.7.1094-b. ISSN 1460-2385.