These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: [X chromosome dominant hereditary nephritis: characterization by pedigree analysis and simple studies in general practice].
    Author: Wälchli P.
    Journal: Praxis (Bern 1994); 1999 Oct 28; 88(44):1811-4. PubMed ID: 10584551.
    Abstract:
    A family with chronic renal disease in the Bernese Oberland (Switzerland) is described. Most family members were directly evaluated by the author. The clinical syndromes identified in different family members are quite variable, reaching from asymptomatic glomerular microhematuria to segmental sclerosing glomerulonephritis with end stage renal failure. Based on the observation of the pedigree over five generations, the disorder appears to be transmitted as an x-chromosomal dominant trait. Together with the ultrastructural diagnosis, the disorder corresponds to an Alport's syndrome Typ IV Atkien.
    [Abstract] [Full Text] [Related] [New Search]