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Delayed diagnosis of homocystinuria presenting with coronavirus disease 2019 in a 17-year-old boy.
Yakut, Nurhayat; Tuzun, Behzat; Ergun, Nurcan Ucuncu.
  • Yakut N; Basaksehir Cam and Sakura City Hospital, Department of Pediatrics, Division of Pediatric Infectious Diseases, Istanbul, Turkey.
  • Tuzun B; Basaksehir Cam and Sakura City Hospital, Department of Pediatric Cardiovascular Surgery, Istanbul, Turkey.
  • Ergun NU; Basaksehir Cam and Sakura City Hospital, Department of Pediatrics, Division of Pediatric Nutrition and Metabolism, Istanbul, Turkey.
Rev Soc Bras Med Trop ; 55: e0143, 2022.
Article in English | MEDLINE | ID: covidwho-2039487
ABSTRACT
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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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Homocystinuria Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid Limits: Adolescent / Humans / Male Language: English Journal: Rev Soc Bras Med Trop Year: 2022 Document Type: Article Affiliation country: 0037-8682-0143-2022

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Homocystinuria Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid Limits: Adolescent / Humans / Male Language: English Journal: Rev Soc Bras Med Trop Year: 2022 Document Type: Article Affiliation country: 0037-8682-0143-2022