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Pierson syndrome

MeSH: C537185ORPHA: 2670

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

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

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with Pierson syndrome, sourced from HPO and Orphanet clinical annotations.

Diffuse mesangial sclerosisCongenital nephrotic syndromeRenal insufficiencyCataractNystagmusMacular hypoplasiaHypotoniaGlobal developmental delayMotor delayOligohydramniosFeeding difficulties in infancyMicrocoriaVisual impairmentHyporeflexiaHypoplasia of the irisRemnants of the hyaloid vascular systemSpherophakia

Classification & Codes

MeSH Code

C537185

Orphanet Code

ORPHA:2670
Pierson syndrome
MeSHC537185
OrphanetORPHA:2670
Treatments0 drug(s)
Symptoms on record17 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO