Literature DB >> 6227247

Turner's syndrome, 46X, del (X) (p 11), persistent complement activation and membranoproliferative glomerulonephritis.

P R Goodyer, J S Fong, B S Kaplan.   

Abstract

An adolescent girl with short stature and learning disability was found to have an unusual variant of Turner's syndrome, 46X, del (X) (p 11) and an abnormal urinary sediment. Further studies demonstrated persistent depression of C3 and histologic evidence of membranoproliferative glomerulonephritis (MPGN). The occurrence of MPGN in this case may have been a manifestation of the known tendency for Turner patients to develop immunologic disease.

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Year:  1982        PMID: 6227247     DOI: 10.1159/000166660

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   3.754


  1 in total

1.  Dialysis modality for patients with Turner syndrome and renal failure.

Authors:  W S Liu; S Y Li; W C Yang; T W Chen; C C Lin
Journal:  Perit Dial Int       Date:  2012 Mar-Apr       Impact factor: 1.756

  1 in total

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