Background. Pierson syndrome (OMIM 609049) is a severe congenital oculorenal disorder with early lethality. The condition is caused by mutations in the LAMB2 gene leading to complete loss of function of the gene product laminin β2, an essential component of the glomerular and other basement membranes. Methods. We present a non-consanguineous family with seven offspring affected by childhood-onset nephrotic syndrome progressing to end-stage renal failure and ocular abnormalities including cataracts, anterior chamber and iris abnormalities, and progressive blindness due to retinal detachment. The LAMB2 gene was analysed in this family by direct sequencing. Results. The disorder turned out to segregate with compoundheterozygosity for two novel LAMB2 mutations, Δ;V79 and Q1728X. Whereas the mutation Q1728X is predicted to confer complete loss of function, ΔV79 probably represents a hypomorphic allele, thus explaining the substantially milder phenotype in this family. Conclusion. This observation demonstrates that the phenotypic spectrum of LAMB2 -associated disorders is broader than previously anticipated, and suggests that milder, non-lethal phenotypes may be associated with mutations retaining some residual function.
|Number of pages||4|
|Journal||Nephrology Dialysis Transplantation|
|Publication status||Published - Nov 2006|
- Autosomal recessive
- Nephrotic syndrome
- Pierson syndrome
ASJC Scopus subject areas