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WT1 gene mutations in three girls with nephrotic syndrome

✍ Scribed by Khalid Ismaili; Véronique Verdure; Katherina Vandenhoute; Françoise Janssen; Michelle Hall

Publisher
Springer
Year
2007
Tongue
English
Weight
70 KB
Volume
167
Category
Article
ISSN
0340-6997

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Congenital nephrotic syndrome, Finnish type (CNF or NPHS1), is an autosomal recessive disease characterized by massive proteinuria and development of nephrotic syndrome shortly after birth. The disease is most common in Finland, but many patients have been identified in other populations. The diseas