CUL3 gene analysis enables early intervention for pediatric pseudohypoaldosteronism type II in infancy

Pediatric Nephrology

Volumn 28, Issue 9, 2013, Pages 1881-1884

  Osawa, Madori ^a   Ogura, Yumi ^a   Isobe, Kiyoshi ^b   Uchida, Shinichi ^b   Nonoyama, Shigeaki ^a   Kawaguchi, Hiroyuki ^a  

^a NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

Cullin 3; Hyperkalemia; Hypertension; Metabolic acidosis; Pseudohypoaldosteronism; Sodium chloride co transporter

Indexed keywords

BICARBONATE; CULLIN 3; ION EXCHANGE RESIN; LIGASE; POTASSIUM; TRICHLORMETHIAZIDE; UNCLASSIFIED DRUG;

ALKALOSIS; ARTICLE; BLOOD GAS ANALYSIS; BODY HEIGHT; BORDERLINE HYPERTENSION; CASE REPORT; CHILD; DIASTOLIC BLOOD PRESSURE; DISEASE COURSE; EARLY INTERVENTION; GENE MUTATION; GENETIC ANALYSIS; GROWTH RETARDATION; HUMAN; HYPERCHLOREMIA; HYPERKALEMIA; INFANT; INFANT DISEASE; LOW BIRTH WEIGHT; MALE; METABOLIC ACIDOSIS; PH; PHENOTYPE; POTASSIUM EXCRETION; PREMATURITY; PRESCHOOL CHILD; PRIORITY JOURNAL; PSEUDOHYPOALDOSTERONISM; PSEUDOHYPOALDOSTERONISM TYPE II; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SYSTOLIC BLOOD PRESSURE; URINARY EXCRETION;

EID: 84881051118     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-013-2496-6     Document Type: Article

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