Karyomegalic interstitial nephritis with a novel FAN1 gene mutation and concurrent ALECT2 amyloidosis

BACKGROUND: Karyomegalic interstitial nephritis (KIN) is a rare hereditary cause of chronic kidney disease. It typically causes progressive renal impairment with haemoproteinuria requiring renal replacement therapy before 50 years of age. It has been associated with mutations in the Fanconi anaemia-...

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Detalles Bibliográficos
Autores principales: Law, Steven, Gillmore, Julian, Gilbertson, Janet A., Bass, Paul, Salama, Alan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049196/
https://www.ncbi.nlm.nih.gov/pubmed/32111193
http://dx.doi.org/10.1186/s12882-020-01733-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049196/
https://www.ncbi.nlm.nih.gov/pubmed/32111193
http://dx.doi.org/10.1186/s12882-020-01733-9

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