Literature DB >> 10603120

Coexistence of thin membrane and alport nephropathies in families with haematuria.

N E Moghal1, D V Milford, R H White, F Raafat, R Higgins.   

Abstract

The finding of familial haematuria without a history of deafness or renal impairment is often assumed to indicate a benign prognosis. However, we describe three families in whom Alport and thin basement membrane nephropathy were separately identified within the same pedigree. Our findings illustrate the importance of fully investigating families with haematuria, even if thin basement nephropathy has been diagnosed in one member.

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Year:  1999        PMID: 10603120     DOI: 10.1007/s004670050699

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  3 in total

1.  The Alport nephropathy: clinicopathological correlations.

Authors:  Richard H R White; Faro Raafat; David V Milford; Filadelfia Komianou; Nadeem E Moghal
Journal:  Pediatr Nephrol       Date:  2005-04-26       Impact factor: 3.714

Review 2.  The role of molecular genetics in diagnosing familial hematuria(s).

Authors:  Constantinos Deltas; Alkis Pierides; Konstantinos Voskarides
Journal:  Pediatr Nephrol       Date:  2011-06-19       Impact factor: 3.714

3.  Pathology vs. molecular genetics: (re)defining the spectrum of Alport syndrome.

Authors:  Jeffrey H Miner
Journal:  Kidney Int       Date:  2014-12       Impact factor: 10.612

  3 in total

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