Literature DB >> 20129018

Familial IgA nephropathy in southeastern Kentucky.

K A Lavigne1, S Y Woodford, C V Barker, B A Julian, J Novak, Z Moldoveanu, A G Gharavi, R J Wyatt.   

Abstract

BACKGROUND: Two decades ago, pedigrees of patients with IgA nephropathy (IgAN) from Pike County, KY, USA, provided evidence for a role of genetic factors in the pathogenesis of this disorder. Subsequently additional pedigrees were described for several communities from northern Italy. Recently, we found another cluster of patients in the Clay County, KY area, about 100 miles southwest of Pike County. AIM: The purpose of this study was to evaluate and expand the pedigrees of patients with IgAN from Clay County, KY to provide additional insight into the mechanisms of inheritance of IgAN and assess the possible influence of a founder effect on the prevalence of IgAN in the region.
METHOD: Since 1980, most patients with IgAN and their relatives in eastern KY have provided personal genealogic data. These data were used to construct pedigrees that included the patients born in Clay County. Nine of 11 patients with IgAN born in Clay County, KY, USA were members of 1 or more of 5 pedigrees, each with 3 - 11 patients with IgAN.
CONCLUSION: Our findings suggest the possibility of a low-penetrance ancestral mutation in the IgAN kindreds from Clay County.

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Year:  2010        PMID: 20129018      PMCID: PMC4116337          DOI: 10.5414/cnp73115

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  28 in total

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2.  Familial clustering of IgA nephropathy: further evidence in an Italian population.

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6.  Regionalization in hereditary IgA nephropathy.

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10.  Iga nephropathy: presentation, clinical course, and prognosis in children and adults.

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Review 6.  IgA vasculitis with nephritis: update of pathogenesis with clinical implications.

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