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Joubert syndrome diagnosed renally late

Joubert syndrome is a genetically heterogeneous multisystem disorder typically diagnosed in childhood. Nephronophthisis is the most common renal pathology in Joubert syndrome, and renal failure usually occurs in childhood or in young adults. We report a 61-year-old female diagnosed with AHI1-related...

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Autores principales: Collard, Elizabeth, Byrne, Catherine, Georgiou, Michalis, Michaelides, Michel, Dixit, Abhijit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986455/
https://www.ncbi.nlm.nih.gov/pubmed/33777383
http://dx.doi.org/10.1093/ckj/sfaa007
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author Collard, Elizabeth
Byrne, Catherine
Georgiou, Michalis
Michaelides, Michel
Dixit, Abhijit
author_facet Collard, Elizabeth
Byrne, Catherine
Georgiou, Michalis
Michaelides, Michel
Dixit, Abhijit
author_sort Collard, Elizabeth
collection PubMed
description Joubert syndrome is a genetically heterogeneous multisystem disorder typically diagnosed in childhood. Nephronophthisis is the most common renal pathology in Joubert syndrome, and renal failure usually occurs in childhood or in young adults. We report a 61-year-old female diagnosed with AHI1-related oculorenal Joubert syndrome, who presented initially with decline in renal function in her 50s. Our report describes exceptionally late presentation of renal disease in Joubert syndrome and highlights the importance of continued renal function monitoring in older adults with Joubert syndrome.
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spelling pubmed-79864552021-03-26 Joubert syndrome diagnosed renally late Collard, Elizabeth Byrne, Catherine Georgiou, Michalis Michaelides, Michel Dixit, Abhijit Clin Kidney J Exceptional Cases Joubert syndrome is a genetically heterogeneous multisystem disorder typically diagnosed in childhood. Nephronophthisis is the most common renal pathology in Joubert syndrome, and renal failure usually occurs in childhood or in young adults. We report a 61-year-old female diagnosed with AHI1-related oculorenal Joubert syndrome, who presented initially with decline in renal function in her 50s. Our report describes exceptionally late presentation of renal disease in Joubert syndrome and highlights the importance of continued renal function monitoring in older adults with Joubert syndrome. Oxford University Press 2020-03-12 /pmc/articles/PMC7986455/ /pubmed/33777383 http://dx.doi.org/10.1093/ckj/sfaa007 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Exceptional Cases
Collard, Elizabeth
Byrne, Catherine
Georgiou, Michalis
Michaelides, Michel
Dixit, Abhijit
Joubert syndrome diagnosed renally late
title Joubert syndrome diagnosed renally late
title_full Joubert syndrome diagnosed renally late
title_fullStr Joubert syndrome diagnosed renally late
title_full_unstemmed Joubert syndrome diagnosed renally late
title_short Joubert syndrome diagnosed renally late
title_sort joubert syndrome diagnosed renally late
topic Exceptional Cases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986455/
https://www.ncbi.nlm.nih.gov/pubmed/33777383
http://dx.doi.org/10.1093/ckj/sfaa007
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AT dixitabhijit joubertsyndromediagnosedrenallylate