Pierson syndrome: a novel cause of congenital nephrotic syndrome.

Abstract

In this report, we describe a newborn infant who presented with congenital nephrotic syndrome and renal insufficiency, as well as bilateral microcoria. This constellation of findings is a hallmark of Pierson syndrome, a newly recognized genetic disorder that is caused by a deficiency of beta2 laminin in the basement membrane. Our patient demonstrated classic histopathologic findings of Pierson syndrome on renal biopsy, including absence of beta2 laminin on immunofluorescent staining, and genetic testing confirmed the diagnosis. We conclude that Pierson syndrome should be included in the differential diagnosis for congenital nephrotic syndrome, especially in patients with ocular abnormalities.

• Authors: Rene' VanDeVoorde, David Witte, Jillene Kogan, Jens Goebel
• Journal: Pediatrics (Pediatrics) Vol. 118 Issue 2 Pg. e501-5 (Aug 2006) ISSN: 1098-4275 [Electronic] United States
• PMID: 16864643 (Publication Type: Case Reports, Journal Article)

Chemical References

• Laminin
• laminin beta2

Topics

• Adult
• Basement Membrane (chemistry)
• Biopsy
• Diagnosis, Differential
• Edema (etiology)
• Female
• Heterozygote
• Humans
• Hypertension, Renal (etiology)
• Infant, Newborn
• Infant, Small for Gestational Age
• Kidney (abnormalities, diagnostic imaging, embryology)
• Kidney Glomerulus (chemistry, ultrastructure)
• Laminin (deficiency, genetics)
• Male
• Mesangial Cells (pathology)
• Miosis (congenital)
• Nephrotic Syndrome (congenital)
• Oligohydramnios (diagnostic imaging)
• Pregnancy
• Syndrome
• Ultrasonography, Prenatal