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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...

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Autores principales: Ghamry, Mohamed A, Salah, Rehab, Galal, Eslam I, Henin, Shereen, Dobs, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
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.
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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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