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Hereditary steroid-resistant nephrotic syndrome

ORPHA:656· ICD-10 N04.1

Definition

A rare, hereditary nephrotic syndrome characterized by proteinuria, hypoalbuminemia, edema, and hyperlipidemia, with an absence of response to an initial trial of corticosteroids (i.e. steroid-resistant nephrotic syndrome; SRNS) and a generally complicated course.

Prevalence
Unknown
Inheritance
Autosomal dominant, Autosomal recessive
Age of onset
Adolescent, Adult, Antenatal, Childhood, Infancy, Neonatal