دورية أكاديمية

A case of CALR mutation in JAK2-negative patient with polycythemia

التفاصيل البيبلوغرافية
العنوان: A case of CALR mutation in JAK2-negative patient with polycythemia
المؤلفون: T. N. Subbotina, I. E. Maslyukova, D. V. Kurochkin, M. A. Mikhalev, M. G. Osadchaya, V. A. Khorzhevskiy, T. A. Garkusha, E. A. Dunaeva, K. O. Mironov
المصدر: Онкогематология, Vol 17, Iss 2, Pp 30-35 (2022)
بيانات النشر: ABV-press, 2022.
سنة النشر: 2022
المجموعة: LCC:Diseases of the blood and blood-forming organs
مصطلحات موضوعية: myeloproliferative neoplasm, polycythemia vera, somatic mutations, jak2-negative status, calr, Diseases of the blood and blood-forming organs, RC633-647.5
الوصف: JAK2 mutations can be associated with any phenotypic form of chronic myeloproliferative neoplasia, while MPL and CALR mutations occur, as a rule, in cases of essential thrombocythemia and primary myelofibrosis and they are not observed in polycythemia vera. In this article we describe a clinical case of CALR mutation (c.1154_1155insGTGTC; p.E386fs*46) presence in a JAK2-negative polycythemia vera patient at age 36. In January 2018 changes in his hemogramm were recorded for the first time. In June 2018, based on a diagnostic study of bone marrow trepanobiopsy, a diagnosis of polycythemia vera was made. Molecular genetic study of the patient’s DNA didn’t reveal mutations in the JAK2 (12 and 14 exons) and the MPL genes. CALR mutation was revealed during the screening by heteroduplex analysis with the electrophoresis in polyacrylamide gel. Then the mutation was identified by Sanger’s DNA sequencing as с.1154_1155insGTGTC; p.E386fs*46. The allelic burden level as determined by pyrosequencing was 20 % (June 2018). In conclusion we can suppose that the revealed CALR mutation с.1154_1155insGTGTC; p.E386fs*46 plays its role in our patient’s polycythemia phenotype.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: Russian
تدمد: 1818-8346
2413-4023
Relation: https://oncohematology.abvpress.ru/ongm/article/view/535; https://doaj.org/toc/1818-8346; https://doaj.org/toc/2413-4023
DOI: 10.17650/1818-8346-2022-17-2-30-35
URL الوصول: https://doaj.org/article/47182056f2d748148f454fefc5457c9c
رقم الأكسشن: edsdoj.47182056f2d748148f454fefc5457c9c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18188346
24134023
DOI:10.17650/1818-8346-2022-17-2-30-35