Artigo Acesso aberto Revisado por pares

Epidemiology of autosomal-dominant polycystic kidney disease: an in-depth clinical study for south-western Germany

2013; Oxford University Press; Volume: 28; Issue: 6 Linguagem: Inglês

10.1093/ndt/gfs551

ISSN

1460-2385

Autores

Hartmut P.H. Neumann, Cordula A. Jilg, Janina Bacher, Zinaida Nabulsi, Angelica Malinoc, Barbara Hummel, Michael M. Hoffmann, Nadina Ortiz-Bruechle, Sven Gläsker, Przemyslaw Pisarski, Hannes Neeff, Annette Krämer‐Guth, Markus Cybulla, Martin Hornberger, Jochen Wilpert, Ludwig Funk, Jörg Baumert, Dietrich Paatz, Dieter Baumann, Markus Lahl, H Felten, Martin Hausberg, Klaus Zerres, Charis Eng,

Tópico(s)

Genetic Syndromes and Imprinting

Resumo

BackgroundAs we emerge into the genomic medicine era, the epidemiology of diseases is taken for granted. Accurate prevalence figures, especially of rare diseases (RDs, ≤50/100 000), will become even more important for purposes of health care and societal planning. We noticed that the numbers of affected individuals in regionally established registries for mainly hereditary RDs do not align with published estimated and expected prevalence figures. We therefore hypothesized that such non-population-based means overestimate RDs and sought to address this by recalculating prevalence for an important 'common' hereditary disease, autosomal-dominant polycystic kidney disease (ADPKD) whereby presumed-prevalence is 100–250/100 000

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