Skip to Accessibility Menu
Skip to Login
Skip to Content
Skip to Footer
Menu
Search
Accessibility
Log in
Subscribe
Congenital nephrotic syndrome, Finnish type
What is Congenital nephrotic syndrome, Finnish type?
A rare congenital nephrotic syndrome characterized by massive protein loss and marked edema manifesting
in utero
or during the first 3 months of life.
Other condition names
Finnish congenital nephrosis
Inheritance type
Autosomal recessive
Prevalence
Worldwide: Unknown
Age of Onset
Antenatal
Infancy
Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.