A Case of Microcephaly and Early-onset Nephrotic Syndrome: Galloway-Mowat Syndrome
Journal of the Korean Society of Pediatric Nephrology
; : 197-203, 2003.
Article
in Korean
| WPRIM (Western Pacific)
| ID: wpr-134296
Responsible library:
WPRO
ABSTRACT
The Galloway-Mowat syndrome, a rare inherited disorder, is characterized by congenital microcephaly with various neurological abnormalities and early onset of nephrotic syndrome with unresponsiveness to treatment, progressive deterioration in renal function and death in early lifetime. In this report, we describe a girl with microcephaly, seizures. and psychomotor retardation who developed nephrotic syndrome at 17 months of age.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Seizures
/
Microcephaly
/
Nephrotic Syndrome
Limits:
Female
/
Humans
Language:
Korean
Journal:
Journal of the Korean Society of Pediatric Nephrology
Year:
2003
Document type:
Article