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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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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. |
format | Online Article Text |
id | pubmed-7986455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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