| Literature DB >> 2739828 |
B Gauthier1, H Trachtman, R Frank, E Valderrama.
Abstract
A review of 130 children with persistent microhematuria showed that the most common abnormality was a form of hereditary nephritis for wich we propose the term 'familial thin basement membrane nephropathy' (FTBMN). This lesion is not as severe as that of Alport's syndrome but carries a guarded prognosis. Family histories, urinalyses and audiograms systematically done on parents and other relatives show that FTBMN may be present in as many as 39% of children with persistent microhematuria and that careful family studies identify children likely to have this lesion.Entities:
Mesh:
Year: 1989 PMID: 2739828 DOI: 10.1159/000185384
Source DB: PubMed Journal: Nephron ISSN: 1660-8151 Impact factor: 2.847