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D. V. Ivanova

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Open access Oct 2026

A personalized approach to the treatment of neonatal diabetes mellitus caused by a KCNJ11 mutation: clinical observations

Neonatal diabetes mellitus (NDM), or diabetes of the newborn, belongs to the group of monogenic forms of the disease and is characterized by marked genetic polymorphism. It is a rare genetically determined disorder with early onset (typically within the first 6 months of life), manifesting as persistent hyperglycemia...

A. Severina, A. O. Emelyanov, T. Kuraeva et al. · 0 citations
Open access Aug 2026

Savelyeva LV. Isolated hypogonadotropic hypogonadism caused by a mutation in the WDR11 gene: a clinical case report

Two clinical cases of patients from the same family with hypogonadotropic hypogonadism caused by a mutation in the WDR11 gene are presented, demonstrating different clinical manifestations and treatment strategies.

D. V. Ivanova, A. N. Zvyagintseva, E. V. Morozova et al. · 0 citations

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