Publications by authors named "Matija Matosevic"

Article Synopsis
  • Nephrotic syndrome (NS) can arise as a rare complication following haematopoietic stem cell transplantation (HSCT), particularly in patients with membranous nephropathy (MN), where the novel antigen protocadherin FAT1 has been identified.
  • A case series at the University Hospital Centre Zagreb tracked three patients who developed NS after HSCT for different types of leukemia, revealing varying kidney function and specific antigen positivity, with two testing positive for FAT1.
  • The study highlights that MN can manifest at different times post-HSCT and emphasizes the significance of antigen testing in understanding the connection between MN and HSCT, suggesting future serum testing for anti-FAT1 antibodies could be beneficial.
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While most countries provide safe and effective influenza vaccines for at-risk groups, influenza vaccine coverage among children with rheumatic diseases remains uncertain. This study investigated influenza vaccination rates in children with juvenile idiopathic arthritis (JIA) during the 2019-2020 season and assessed the knowledge and attitudes of caregivers of children with JIA regarding influenza vaccination. The secondary aims were to identify barriers to vaccination and explore strategies to improve vaccination rates.

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Introduction: As the global pandemic continues, new complications of COVID-19 in pediatric population have turned up, one of them being hemolytic uremic syndrome (HUS), a complement-mediated thrombotic microangiopathy (CM-TMA) characterized by triad of thrombocytopenia, microangiopathic hemolytic anemia and acute kidney injury (AKI). With both multisystem inflammatory syndrome in children (MIS-C) and HUS sharing complement dysregulation as one of the key factors, the aim of this case report is to highlight differences between these two conditions and also emphasize the importance of complement blockade as a treatment modality.

Case Report: We describe a 21-month-old toddler who initially presented with fever and confirmed COVID-19.

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Camptodactyly and clinodactyly are most commonly considered just cosmetic defects, but they can pose a major diagnostic and therapeutic challenge, mainly because of their apparently similar clinical presentation. For years, experts have been arguing over definitions, descriptions, and therapeutic approaches to these deformities, with some favoring surgical approach, some advocating conservative treatment, while others are prone to use a combination of the aforementioned approaches. This article provides an overview of the current literature on two different entities, with emphasis on differences in clinical presentation and treatment modalities.

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