Corrigendum: A clinical case of pregnancy of a patient with a combination of two orphan diseases: familial partial lipodystrophy type 4 and hnf1a-mody on the background of therapy with recombinant human methionyl leptin (Diabetes mellitus. 2025;28(3). doi: 10.14341/DM13333)

N. V. Frolkova; E. R. Radkevich; E. O. Koksharova; F. F. Burumkulova; P. A. Vasiluev; I. R. Minniakhmetov; I. A. Eremina; M. V. Shestakova

doi:10.14341/DM13409

Corrigendum: A clinical case of pregnancy of a patient with a combination of two orphan diseases: familial partial lipodystrophy type 4 and hnf1a-mody on the background of therapy with recombinant human methionyl leptin (Diabetes mellitus. 2025;28(3). doi: 10.14341/DM13333)

N. V. Frolkova, E. R. Radkevich, E. O. Koksharova, F. F. Burumkulova, P. A. Vasiluev, I. R. Minniakhmetov, I. A. Eremina, M. V. Shestakova

https://doi.org/10.14341/DM13409

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Abstract

An error was identified in the article “A clinical case of pregnancy of a patient with a combination of two orphan diseases: familial partial lipodystrophy type 4 and HNF1A-MODY on the background of therapy with recombinant human methionyl leptin” by Frolkova N.V., Radkevich E.R., Koksharova E.O., Burumkulova F.F., Vasiliev P.A., Minniakhmetov I.R., Eremina I.A., Shestakova M.V., published in Diabetes mellitus. 2025;28(3):305-315. doi: https://doi.org/10.14341/DM13333. An error was made in the article: the source of funding was incorrectly indicated in the final text. The correct funding source is: This work was carried out within the framework of the state assignment «Model for personalized risk prediction of diabetes mellitus in children based on molecular genetic markers in ethnic groups of the Russian Federation and in familial cases of the disease,» state registration number 123021000040-9.

Keywords

hereditary lipodystrophies, familial partial lipodystrophy, diabetes mellitus, MODY 3, PLIN1, HNF1A, pregnancy, orphan diseases, metreleptin, fertility

For citations:

Frolkova N.V., Radkevich E.R., Koksharova E.O., Burumkulova F.F., Vasiluev P.A., Minniakhmetov I.R., Eremina I.A., Shestakova M.V. Corrigendum: A clinical case of pregnancy of a patient with a combination of two orphan diseases: familial partial lipodystrophy type 4 and hnf1a-mody on the background of therapy with recombinant human methionyl leptin (Diabetes mellitus. 2025;28(3). doi: 10.14341/DM13333). Diabetes mellitus. 2025;28(5):487-488. (In Russ.) https://doi.org/10.14341/DM13409

An error was made in the article: the source of funding was incorrectly indicated in the final text.

The correct funding source is: This work was carried out within the framework of the state assignment «Model for personalized risk prediction of diabetes mellitus in children based on molecular genetic markers in ethnic groups of the Russian Federation and in familial cases of the disease,» state registration number 123021000040-9.

The editorial office regrets the error. The original version of the article has been replaced.