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Alport's Syndrome: A Rare Clinical Presentation with Crescents
Alport's syndrome (hereditary nephritis) is a familial disorder, which usually affects young males with clinical presentation of hematuric and glomerular disease. We report a rare case of Alport's syndrome in a 16-year-old male with typical extrarenal manifestations and renal biopsy findin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132844/ https://www.ncbi.nlm.nih.gov/pubmed/32269440 http://dx.doi.org/10.4103/ijn.IJN_177_19 |
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author | Haldar, Ishani Jeloka, Tarun |
author_facet | Haldar, Ishani Jeloka, Tarun |
author_sort | Haldar, Ishani |
collection | PubMed |
description | Alport's syndrome (hereditary nephritis) is a familial disorder, which usually affects young males with clinical presentation of hematuric and glomerular disease. We report a rare case of Alport's syndrome in a 16-year-old male with typical extrarenal manifestations and renal biopsy findings with crescents. |
format | Online Article Text |
id | pubmed-7132844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-71328442020-04-08 Alport's Syndrome: A Rare Clinical Presentation with Crescents Haldar, Ishani Jeloka, Tarun Indian J Nephrol Case Report Alport's syndrome (hereditary nephritis) is a familial disorder, which usually affects young males with clinical presentation of hematuric and glomerular disease. We report a rare case of Alport's syndrome in a 16-year-old male with typical extrarenal manifestations and renal biopsy findings with crescents. Wolters Kluwer - Medknow 2020 2020-02-07 /pmc/articles/PMC7132844/ /pubmed/32269440 http://dx.doi.org/10.4103/ijn.IJN_177_19 Text en Copyright: © 2020 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Haldar, Ishani Jeloka, Tarun Alport's Syndrome: A Rare Clinical Presentation with Crescents |
title | Alport's Syndrome: A Rare Clinical Presentation with Crescents |
title_full | Alport's Syndrome: A Rare Clinical Presentation with Crescents |
title_fullStr | Alport's Syndrome: A Rare Clinical Presentation with Crescents |
title_full_unstemmed | Alport's Syndrome: A Rare Clinical Presentation with Crescents |
title_short | Alport's Syndrome: A Rare Clinical Presentation with Crescents |
title_sort | alport's syndrome: a rare clinical presentation with crescents |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132844/ https://www.ncbi.nlm.nih.gov/pubmed/32269440 http://dx.doi.org/10.4103/ijn.IJN_177_19 |
work_keys_str_mv | AT haldarishani alportssyndromearareclinicalpresentationwithcrescents AT jelokatarun alportssyndromearareclinicalpresentationwithcrescents |