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Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy

Homocystinuria is a treatable autosomal recessive inherited disorder. This condition may cause life-threatening complications such as thromboembolic events. Coronavirus disease 2019 (COVID-19) is associated with an increased risk of venous thromboembolic events. Here, we report a case of late diagno...

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Autores principales: Yakut, Nurhayat, Tuzun, Behzat, Ergun, Nurcan Ucuncu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical - SBMT 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549948/
https://www.ncbi.nlm.nih.gov/pubmed/36134859
http://dx.doi.org/10.1590/0037-8682-0143-2022
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author Yakut, Nurhayat
Tuzun, Behzat
Ergun, Nurcan Ucuncu
author_facet Yakut, Nurhayat
Tuzun, Behzat
Ergun, Nurcan Ucuncu
author_sort Yakut, Nurhayat
collection PubMed
description Homocystinuria is a treatable autosomal recessive inherited disorder. This condition may cause life-threatening complications such as thromboembolic events. Coronavirus disease 2019 (COVID-19) is associated with an increased risk of venous thromboembolic events. Here, we report a case of late diagnosis of homocystinuria presenting with deep venous thrombosis and COVID-19. This study highlights a sustained high index of suspicion for homocystinuria to prevent severe thromboembolic complications.
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spelling pubmed-95499482022-10-25 Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy Yakut, Nurhayat Tuzun, Behzat Ergun, Nurcan Ucuncu Rev Soc Bras Med Trop Case Report Homocystinuria is a treatable autosomal recessive inherited disorder. This condition may cause life-threatening complications such as thromboembolic events. Coronavirus disease 2019 (COVID-19) is associated with an increased risk of venous thromboembolic events. Here, we report a case of late diagnosis of homocystinuria presenting with deep venous thrombosis and COVID-19. This study highlights a sustained high index of suspicion for homocystinuria to prevent severe thromboembolic complications. Sociedade Brasileira de Medicina Tropical - SBMT 2022-09-19 /pmc/articles/PMC9549948/ /pubmed/36134859 http://dx.doi.org/10.1590/0037-8682-0143-2022 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Case Report
Yakut, Nurhayat
Tuzun, Behzat
Ergun, Nurcan Ucuncu
Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
title Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
title_full Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
title_fullStr Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
title_full_unstemmed Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
title_short Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
title_sort delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549948/
https://www.ncbi.nlm.nih.gov/pubmed/36134859
http://dx.doi.org/10.1590/0037-8682-0143-2022
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