Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis

Pediatric Nephrology

Volumn 24, Issue 2, 2009, Pages 415-418

  Yamazaki, Hajime ^a   Nozu, Kandai ^b   Narita, Ichiei ^c   Nagata, Michio ^d   Nozu, Yoshimi ^b   Fu, Xue Jun ^b   Matsuo, Masafumi ^b   Iijima, Kazumoto ^b   Gejyo, Fumitake ^c  

^a NAGAOKA RED CROSS HOSPITAL   (Japan)

^b KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c NIIGATA UNIVERSITY   (Japan)

^d UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

Bartter syndrome; Focal segmental glomerulosclerosis; Late onset; NKCC2; SLC12A1

Indexed keywords

ALANINE; GLYCINE; PROTEIN SLC12A1; SODIUM POTASSIUM CHLORIDE COTRANSPORTER; UNCLASSIFIED DRUG; VALINE;

ADULT; ARTICLE; BARTTER SYNDROME; CASE REPORT; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DISEASE SEVERITY; FOCAL GLOMERULOSCLEROSIS; GENE MUTATION; GENETIC SCREENING; HETEROZYGOTE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; JUXTAGLOMERULAR APPARATUS; KIDNEY BIOPSY; KIDNEY CALCIFICATION; KIDNEY FAILURE; LABORATORY TEST; MALE; METABOLIC ALKALOSIS; MUTATIONAL ANALYSIS; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PROTEINURIA;

ADULT; AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; BARTTER SYNDROME; BIOPSY; FAMILY HEALTH; FEMALE; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PHENOTYPE; SODIUM-POTASSIUM-CHLORIDE SYMPORTERS;

EID: 58149094899     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-008-0999-3     Document Type: Article

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