Glomerulopathy in patients with distal duplication of chromosome 6p

BACKGROUND: Duplication of the distal part of chromosome 6p is a rare genetic syndrome. Renal involvement has been reported in the majority of patients, including a wide range of congenital abnormalities of kidney and urinary tract and, occasionally, a proteinuric glomerulopathy. CASE PRESENTATION:...

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Detalles Bibliográficos
Autores principales: Jankauskienė, Augustina, Koczkowska, Magdalena, Bjerre, Anna, Bernaciak, Joanna, Schaefer, Franz, Lipska-Ziętkiewicz, Beata S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802583/
https://www.ncbi.nlm.nih.gov/pubmed/27000031
http://dx.doi.org/10.1186/s12882-016-0246-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802583/
https://www.ncbi.nlm.nih.gov/pubmed/27000031
http://dx.doi.org/10.1186/s12882-016-0246-2

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