Immunodeficiency and hemolytic uremic syndrome: a case report

This case highlights the increased susceptibility of individuals with A-T to infections and the potential for life-threatening complications, such as HUS. The coexistence of A-T and STEC-HUS presentes unique challenges in diagnosis and management. Early recognition and targeted treatment led to a successful recovery and underscored the importance of close follow-up in immunodeficient patients.

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Publication Details

Journal
The Turkish Journal of Pediatrics
Published
2025-10-20
DOI
https://doi.org/10.24953/turkjpediatr.2025.5614
Primary Topic
Complement system in diseases
Type
article
Field-Weighted Citation Impact
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article

Immunodeficiency and hemolytic uremic syndrome: a case report

Nihal Akçay, İlyas Bingöl, Demet Tosun
The Turkish Journal of Pediatrics
Complement system in diseases
article

Immunodeficiency and hemolytic uremic syndrome: a case report

Nihal Akçay, İlyas Bingöl, Demet Tosun
article en

Abstract

This case highlights the increased susceptibility of individuals with A-T to infections and the potential for life-threatening complications, such as HUS. The coexistence of A-T and STEC-HUS presentes unique challenges in diagnosis and management. Early recognition and targeted treatment led to a successful recovery and underscored the importance of close follow-up in immunodeficient patients.

The Turkish Journal of PediatricsVol. 67(5)
Sağlık Bilimleri Üniversitesi (TR), İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi (TR)
Openalex Percentile: Top 69%
Complement system in diseases
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