Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay

Clinical Dysmorphology

Volumn 10, Issue 2, 2001, Pages 115-121

  De Vries, Bert B A ^a,b,c   Van't Hoff, William G ^a,b,c   Surtees, Robert A H ^a,b,c   Winter, Robin M ^a,b,c  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

ARC syndrome; CDG syndrome; Developmental delay; Galloway Mowat syndrome; Microcephaly; Nephrotic syndrome; PEHO syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLINICAL EXAMINATION; CONGENITAL DISORDER OF GLYCOSYLATION; CONGENITAL NEPHROTIC SYNDROME; DEVELOPMENTAL DISORDER; DIFFERENTIAL DIAGNOSIS; FEMALE; GALLOWAY MOWAT SYNDROME; HUMAN; INFANT; MALFORMATION SYNDROME; MICROCEPHALY; PRESCHOOL CHILD; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0035084998     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200104000-00008     Document Type: Article

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