Genetic mutations and response to immunosuppressive therapy in paediatric steroid-resistant nephrotic syndrome

Mutaciones genéticas y respuesta a la terapia inmunosupresora en el síndrome nefrótico pediátrico resistente a esteroides

Introduction: The prevalence of congenital nephrotic syndrome, affecting approximately 1 in 6,000 newborns, underscores the relevance of this study. This research involved 15 children with steroid-resistant nephrotic syndrome (SRNS), 9 of whom underwent nephrobiopsy. Objective: To evaluate the genetic conditionality of SRNS and the prognostic significance of immunosuppressive therapy.

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Книга Публикация научной статьи Волощук 2026 Book Publication of a scientific article 2026