Cargando…
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome
BACKGROUND: Joubert syndrome (JS) is an inherited ciliopathy characterized by a complex midbrain–hindbrain malformation and multiorgan involvement. Renal disease, mainly juvenile nephronophthisis (NPH), was reported in 25–30% patients although only ∼18% had a confirmed diagnosis of chronic kidney di...
Autores principales: | Nuovo, Sara, Fuiano, Laura, Micalizzi, Alessia, Battini, Roberta, Bertini, Enrico, Borgatti, Renato, Caridi, Gianluca, D’Arrigo, Stefano, Fazzi, Elisa, Fischetto, Rita, Ghiggeri, Gian Marco, Giordano, Lucio, Leuzzi, Vincenzo, Romaniello, Romina, Signorini, Sabrina, Stringini, Gilda, Zanni, Ginevra, Romani, Marta, Valente, Enza Maria, Emma, Francesco |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417010/ https://www.ncbi.nlm.nih.gov/pubmed/30403813 http://dx.doi.org/10.1093/ndt/gfy333 |
Ejemplares similares
-
Age and sex prevalence estimate of Joubert syndrome in Italy
por: Nuovo, Sara, et al.
Publicado: (2020) -
Recurrent, founder and hypomorphic variants contribute to the genetic landscape of Joubert syndrome
por: Serpieri, Valentina, et al.
Publicado: (2023) -
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum
por: Serpieri, Valentina, et al.
Publicado: (2022) -
Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders
por: Romaniello, Romina, et al.
Publicado: (2022) -
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
por: Roosing, Susanne, et al.
Publicado: (2016)