Focal segmental glomerulosclerosis, Coats'-like retinopathy, sensorineural deafness and chromosome 4 duplication: A new association

Pediatric Nephrology

Volumn 25, Issue 8, 2010, Pages 1551-1554

  Reynolds, Ben C ^a   Lemmers, Richard J L F ^b   Tolmie, John ^a   Howatson, Allan G ^a   Hughes, David A ^a  

^a ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Genetic inheritance; Glomerulonephritis; Nephrotic syndrome

Indexed keywords

ENALAPRIL; PREDNISOLONE;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4Q; CHROMOSOME DUPLICATION; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; DYSTROPHY; EXUDATIVE RETINITIS; FAHR DISEASE; FASCIOSCAPULOHUMERAL DYSTROPHY; FEMALE; FOCAL GLOMERULOSCLEROSIS; GENETIC ASSOCIATION; HEARING IMPAIRMENT; HUMAN; NEPHROTIC SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; CHROMOSOME 4; FOLLOW UP; GENETICS; PERCEPTION DEAFNESS; RETINA DISEASE; TIME;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; FOLLOW-UP STUDIES; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HEARING LOSS, SENSORINEURAL; HUMANS; NEPHROTIC SYNDROME; RETINAL DISEASES; TIME FACTORS;

EID: 77954425613     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-010-1474-5     Document Type: Article

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