Cargando…
New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene
BACKGROUND: Karyomegalic interstitial nephritis (KIN) is a rare disease entity first described by Burry in 1974. The term KIN was introduced by Mihatsch et al. in 1979. KIN is characterized by chronic tubulointerstitial nephritis associated with enlarged tubular epithelial cell nuclei, which leads t...
Autores principales: | Rejeb, Imen, Jerbi, Mouna, Jilani, Houweyda, Gaied, Hanène, Elaribi, Yasmina, Hizem, Syrine, Aoudia, Raja, Hedri, Hafedh, Zaied, Chiraz, Abid, Salwa, Bacha, Hassen, BenAbdallah, Taieb, BenJemaa, Lamia, Goucha, Rim |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201669/ https://www.ncbi.nlm.nih.gov/pubmed/34126972 http://dx.doi.org/10.1186/s12920-021-01009-7 |
Ejemplares similares
-
Encapsulating Peritoneal Sclerosis after kidney Transplantation: Success of Medical Treatment
por: Gaied, Hanene, et al.
Publicado: (2021) -
Renal Thrombotique microangiopathy: An unusual renal involvement in Niemann‐Pick disease type B
por: Jerbi, Mouna, et al.
Publicado: (2020) -
A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report
por: Jilani, Houweyda, et al.
Publicado: (2022) -
First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations
por: Rejeb, Imen, et al.
Publicado: (2017) -
Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature
por: Sassi, Hela, et al.
Publicado: (2021)