Pierson syndrome

MONDO:0012184

Pierson syndrome is characterized by the association of congenital nephrotic syndrome and ocular anomalies with microcoria.

Also known as: Pierson syndrome, microcoria-congenital nephrosis syndrome, microcoria - congenital nephrosis, microcoria - congenital nephrotic syndrome, microcoria-congenital nephrotic syndrome

4 clinical trials for this condition and its sub-types, 0 tagged with Pierson syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive disease (999) ↑ LAMB2-related infantile-onset nephrotic syndrome (0)

Including sub-types (4) Tagged with Pierson syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.