| Literature DB >> 29532936 |
F Anglani1, L Terrin1, M Brugnara2, M Battista3, V Cantaluppi3, M Ceol1, L Bertoldi4, G Valle4, M P Joy5, B R Pober5, M Longoni5.
Abstract
Whole exome sequencing detected novel likely pathogenic variants in LRP2 gene in 2 patients presenting with hearing and vision loss, and the Dent disease (DD) classical renal phenotype, that is, low molecular weight proteinuria (LMWP), hypercalciuria and nephrocalcinosis/nephrolithiasis. We propose that a subset of patients presenting as DD may represent unrecognized cases or mild forms of Donnai-Barrow/facio-oculo-acustico-renal (DB/FOAR) syndrome or be on the phenotypic continuum between the 2 conditions.Entities:
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Year: 2018 PMID: 29532936 PMCID: PMC5995642 DOI: 10.1111/cge.13242
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438