A case report of familial renal hypouricemia confirmed by genotyping of SLC22A12, and a literature review

Electrolyte and Blood Pressure

Volumn 13, Issue 2, 2015, Pages 52-57

  Kim, Hyung Oh ^a   Ihm, Chun Gyoo ^a   Jeong, Kyung Hwan ^a   Kang, Hyun Joon ^a   Kim, Jae Min ^a   Lim, Hyung Suk ^a   Kim, Jin Sug ^a   Lee, Tae Won ^a  

^a Kyung Hee University Hospital   (South Korea)

Author keywords

Acute kidney injury; Familial renal hypouricemia; SLC22A12; URAT1

Indexed keywords

CREATININE; URATE TRANSPORTER; URIC ACID;

ACUTE KIDNEY FAILURE; ADULT; ANAMNESIS; ARTICLE; BIOCHEMISTRY; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; CREATININE BLOOD LEVEL; EXERCISE; FAMILIAL RENAL HYPOURICEMIA; FAMILY; FLANK PAIN; FLUID THERAPY; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HOMOZYGOSITY; HOSPITALIZATION; HUMAN; HYPOURICEMIA; IMAGE ANALYSIS; KOREAN (PEOPLE); MALE; SEQUENCE ANALYSIS; URIC ACID BLOOD LEVEL; UROLITHIASIS;

EID: 84957098792     PISSN: 17385997     EISSN: 20929935     Source Type: Journal    
DOI: 10.5049/EBP.2015.13.2.52     Document Type: Article

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