Familial IPEX syndrome: Different glomerulopathy in two siblings

Pediatrics International

Volumn 57, Issue 2, 2015, Pages e59-e61

  Park, Eujin ^a   Chang, Hye Jin ^a   Shin, Jae Il ^b   Lim, Beom Jin ^b   Jeong, Hyeon Joo ^b   Lee, Kyoung Bun ^c   Moon, Kyoung Chul ^c   Kang, Hee Gyung ^a,c   Ha, Il Soo ^a,d   Cheong, Hae Il ^a,c,d  

^a Seoul National University Children's Hospital   (South Korea)

^b Yonsei University College of Medicine   (South Korea)

^c Seoul National University Hospital   (South Korea)

^d Seoul National University   (South Korea)

Author keywords

FOXP3; IPEX syndrome; membranous nephropathy; minimal change nephrotic syndrome; regulatory T cell

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4; CREATININE; CYCLOSPORIN; METHOTREXATE; NEUTROPHIL CYTOPLASMIC ANTIBODY; SERUM ALBUMIN; STEROID; TACROLIMUS; THYROXINE; TRANSCRIPTION FACTOR FOXP3; FORKHEAD TRANSCRIPTION FACTOR; FOXP3 PROTEIN, HUMAN;

ARTICLE; CASE REPORT; CELL INFILTRATION; CHILD; CONGENITAL HYPOTHYROIDISM; COOMBS TEST; CREATININE BLOOD LEVEL; DEATH; DESQUAMATION; DIARRHEA; DISEASE COURSE; DRUG ERUPTION; DRUG SUBSTITUTION; DRUG WITHDRAWAL; DUODENUM BIOPSY; EPSTEIN BARR VIRUS INFECTION; FACE EDEMA; FAMILIAL DISEASE; FIBROSING ALVEOLITIS; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HEMOLYTIC ANEMIA; HEPATIC ENCEPHALOPATHY; HEPATITIS; HUMAN; HUMAN TISSUE; IMMUNOFLUORESCENCE; IPEX SYNDROME; KIDNEY BIOPSY; MALE; MEMBRANOUS GLOMERULONEPHRITIS; MINIMAL CHANGE NEPHROTIC SYNDROME; MONONUCLEAR CELL; NEPHROTIC SYNDROME; NEPHROTOXICITY; NEWBORN SCREENING; PATIENT MONITORING; PETECHIA; PIGMENT DISORDER; PRIORITY JOURNAL; PROTEINURIA; PRURITUS; RARE DISEASE; SEPTIC SHOCK; THROMBOCYTOPENIA; URINALYSIS; DIABETES MELLITUS, TYPE 1; GENETIC DISEASES, X-LINKED; GENETICS; GLOMERULONEPHRITIS, MEMBRANOUS; IMMUNE SYSTEM DISEASES; KIDNEY; MUTATION; NEPHROSIS, LIPOID; NEWBORN; PATHOLOGY; PRESCHOOL CHILD; SIBLING;

CHILD, PRESCHOOL; DIABETES MELLITUS, TYPE 1; DIARRHEA; FORKHEAD TRANSCRIPTION FACTORS; GENETIC DISEASES, X-LINKED; GLOMERULONEPHRITIS, MEMBRANOUS; HUMANS; IMMUNE SYSTEM DISEASES; INFANT, NEWBORN; KIDNEY; MALE; MUTATION; NEPHROSIS, LIPOID; SIBLINGS;

EID: 84927602149     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/ped.12570     Document Type: Article

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