Renal hypouricemia

Common Name(s)

Renal hypouricemia

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Renal hypouricemia" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Renal hypouricemia" returned 14 free, full-text research articles on human participants. First 3 results:

Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity.
 

Author(s): Guido Jeannin, Nicola Chiarelli, Mario Gaggiotti, Marco Ritelli, Paolo Maiorca, Stefano Quinzani, Federica Verzeletti, Stefano Possenti, Marina Colombi, Giovanni Cancarini

Journal:

 

Familial renal hypouricemia (RHUC) is a hereditary disease characterized by hypouricemia, high renal fractional excretion of uric acid (FE-UA) and can be complicated by acute kidney failure and nephrolithiasis. Loss-of-function mutations in the SLC22A12 gene cause renal hypouricemia ...

Last Updated: 13 Jan 2014

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Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.
 

Author(s): Blanka Stiburkova, Ivan Sebesta, Kimiyoshi Ichida, Makiko Nakamura, Helena Hulkova, Vladimir Krylov, Lenka Kryspinova, Helena Jahnova

Journal: Eur. J. Hum. Genet.. 2013 Oct;21(10):1067-73.

 

Renal hypouricemia (RHUC) is a heterogeneous inherited disorder characterized by impaired tubular uric acid (UA) transport with severe complications, such as acute kidney injury (AKI). Type 1 is caused by a loss-of-function mutation in the SLC22A12 gene (URAT1), type 2 in the SLC2A9 ...

Last Updated: 19 Sep 2013

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A case of exercise-induced acute renal failure with G774A mutation in SCL22A12 causing renal hypouricemia.
 

Author(s): Yong Hyun Kim, Jong Tae Cho

Journal: J. Korean Med. Sci.. 2011 Sep;26(9):1238-40.

 

Acute renal failure with severe loin pain which develops after anaerobic exercise is rare. One of predisposing factors of exercise-induced acute renal failure is renal hypouricemia. Idiopathic renal hypouricemia is a genetic disorder characterized by hypouricemia with abnormally high ...

Last Updated: 21 Sep 2011

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Renal hypouricemia" returned 1 free, full-text review articles on human participants. First 3 results:

Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review.
 

Author(s): Huijun Shen, Chunyue Feng, Xia Jin, Jianhua Mao, Haidong Fu, Weizhong Gu, Ai'min Liu, Qiang Shu, Lizhong Du

Journal:

 

Idiopathic renal hypouricemia (iRHUC) is an autosomal recessive hereditary disorder, characterized by impaired tubular uric acid transport, re-absorption insufficiency and/or the acceleration of secretions. Some patients present with severe complications, such as exercise-induced ...

Last Updated: 20 Mar 2014

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.