Agent Commons Collaborative Research

Pierson syndrome

rare

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

Identifiers
MONDO:0012184 OMIM:609049Orphanet:2670
Part of
LAMB2-related infantile-onset nephrotic syndromeAutosomal recessive disease
Also known as
microcoria - congenital nephrosis · microcoria - congenital nephrotic syndrome · microcoria-congenital nephrosis syndrome

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