Antinuclear antibodies in children with Wilson’s disease

Author:

Kurbatova O. V.1,Zhuzhula A. A.1,Lapin S. V.2,Snovskaya M. A.1,Kozlova D. I.3,Petrichuk S. V.1,Kuptsova D. G.1,Kuznetsova D. A.2,Movsisyan G. B.1,Komarova A. D.1,Radygina T. V.1,Guslev A. B.4,Kholopova I. V.2,Semikina E. L.5,Makarova S. G.6,Potapov A. S.5,Fisenko A. P.1

Affiliation:

1. National Medical Research Center for Children’s Health

2. Federal State Budgetary Educational Institution of Higher Education PSPbSMU named after acad. I. P. Pavlova Ministry of Health of Russia

3. Federal State Budgetary Healthcare Institution St. Petersburg Clinical Hospital 1 of the Russian Academy of Sciences; Federal State Budgetary Institution of Science Institute of Evolutionary Physiology and Biochemistry named after I. M. Sechenov Russian Academy of Sciences

4. Federal State Budgetary Educational Institution of Higher Education PSPbSMU named after acad. I. P. Pavlova Ministry of Health of Russia; Federal State Budgetary Healthcare Institution St. Petersburg Clinical Hospital 1 of the Russian Academy of Sciences

5. National Medical Research Center for Children’s Health; Sechenov First Moscow State Medical University

6. National Medical Research Center for Children’s Health; Lomonosov Moscow State University

Abstract

.

Publisher

Association of Pediatric Allergologists and Immunologists of Russia

Reference21 articles.

1. Fisenko AP, Surkov AN, Potapov AS. Wilson’s disease in children. M: National Medical Research Center for Children’s Health, 2019. — P. 84. (In Russ.)

2. Lucena-Valera A, Ruz-Zafra P, Ampuero J. Wilson’s disease: overview. Enfermedad de Wilson. Med Clin (Barc). 2023; 160 (6): 261–267. doi: 10.1016/j.medcli.2022.12.016.

3. Lu ZK et al. Phenotypes and ATP7B gene variants in 316 children with Wilson disease. Zhonghua Er Ke Za Zhi. 2022; 60 (4): 317–322. doi: 10.3760/cma.j.cn112140-20210827-00708.

4. Baiazutdinova GM, Shchagina OA, Poliakov AV. The study of common mutation p.H1069Q in АТР7В gene in Russian WD-patients. Medical Genetics. 2018; 17 (4): 25–30. (In Russ.) URL: https://www.medgen-journal.ru/jour/article/view/429?locale=ru_RU.

5. Postrigan AE, Zhalsanova IZh, Fonova EA, Skryabin NA. Modifier genes as the cause of clinical polymorphism of Wilson — Konovalov disease. Genetics. 2021; 57 (5): 516–527. (In Russ.) doi: 10.31857/S001667582105009X.

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