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A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure
Wiedemann-Rautenstrauch Syndrome (WRS), also known as neonatal progeroid syndrome, is an extremely rare genetic syndrome characterized by a senile appearance at birth with multiple complex symptoms. We reported a case of a three-days old male neonate with features of WRS presented with fatal hyperka...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484294/ https://www.ncbi.nlm.nih.gov/pubmed/36159344 http://dx.doi.org/10.7759/cureus.29320 |
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author | Ghamry, Mohamed A Salah, Rehab Galal, Eslam I Henin, Shereen Dobs, Monica |
author_facet | Ghamry, Mohamed A Salah, Rehab Galal, Eslam I Henin, Shereen Dobs, Monica |
author_sort | Ghamry, Mohamed A |
collection | PubMed |
description | Wiedemann-Rautenstrauch Syndrome (WRS), also known as neonatal progeroid syndrome, is an extremely rare genetic syndrome characterized by a senile appearance at birth with multiple complex symptoms. We reported a case of a three-days old male neonate with features of WRS presented with fatal hyperkalemic renal failure which is a unique presentation not reported before in the cases affected with this syndrome. There is a positive family history of a previous sibling with the same features who suddenly died during the first week of life. This case report aimed to increase the awareness of WRS about the features and the importance of close follow-up of the affected cases, especially in the neonatal period among neonatal physicians. |
format | Online Article Text |
id | pubmed-9484294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-94842942022-09-22 A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure Ghamry, Mohamed A Salah, Rehab Galal, Eslam I Henin, Shereen Dobs, Monica Cureus Genetics Wiedemann-Rautenstrauch Syndrome (WRS), also known as neonatal progeroid syndrome, is an extremely rare genetic syndrome characterized by a senile appearance at birth with multiple complex symptoms. We reported a case of a three-days old male neonate with features of WRS presented with fatal hyperkalemic renal failure which is a unique presentation not reported before in the cases affected with this syndrome. There is a positive family history of a previous sibling with the same features who suddenly died during the first week of life. This case report aimed to increase the awareness of WRS about the features and the importance of close follow-up of the affected cases, especially in the neonatal period among neonatal physicians. Cureus 2022-09-19 /pmc/articles/PMC9484294/ /pubmed/36159344 http://dx.doi.org/10.7759/cureus.29320 Text en Copyright © 2022, Ghamry et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Genetics Ghamry, Mohamed A Salah, Rehab Galal, Eslam I Henin, Shereen Dobs, Monica A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure |
title | A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure |
title_full | A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure |
title_fullStr | A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure |
title_full_unstemmed | A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure |
title_short | A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Failure |
title_sort | case of wiedemann-rautenstrauch syndrome with fatal hyperkalemic renal failure |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484294/ https://www.ncbi.nlm.nih.gov/pubmed/36159344 http://dx.doi.org/10.7759/cureus.29320 |
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