Cargando…
Unique Combination of Diamond–Blackfan Anemia and Lynch Syndrome in Adult Female: A Case Report
We present an extremely rare clinical case of a 38-year-old Russian patient with multiple malignant neoplasms of the uterus and colon caused by genetically confirmed two hereditary diseases: Diamond–Blackfan anemia and Lynch syndrome. Molecular genetic research carried out by various methods (NGS, S...
Autores principales: | Tsukanov, Aleksey S., Pikunov, Dmitriy Y., Shubin, Vitaly P., Barinov, Aleksey A., Kashnikov, Vladimir N., Shelygin, Yuri A., Kaprin, Andrey D., Filonenko, Elena V., Sidorov, Dmitriy V., Maschan, Aleksey A., Novichkova, Galina A., Yasko, Liudmila A., Raykina, Elena V., Rumyantsev, Aleksandr G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085342/ https://www.ncbi.nlm.nih.gov/pubmed/33937060 http://dx.doi.org/10.3389/fonc.2021.652696 |
Ejemplares similares
-
Epithelial-Mesenchymal Transition and Somatic Alteration in Colorectal Cancer with and without Peritoneal Carcinomatosis
por: Shelygin, Y. A., et al.
Publicado: (2014) -
Microsatellite Instability in Russian Patients with Colorectal Cancer
por: Shubin, Vitaly, et al.
Publicado: (2022) -
BTK, NUTM2A, and PRPF19 Are Novel KMT2A Partner Genes in Childhood Acute Leukemia
por: Zerkalenkova, Elena, et al.
Publicado: (2021) -
RARE-52. RB1 GENE DELETIONS ARE THE NOVEL MECHANISM OF CHOROID PLEXUS TUMORS (CPT) ONCOGENESIS
por: Druy, Alexander, et al.
Publicado: (2020) -
Altered translation of GATA1 in Diamond-Blackfan anemia
por: Ludwig, Leif S., et al.
Publicado: (2014)