Zobrazeno 1 - 10
of 1 993
pro vyhledávání: '"trisomy 8"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
ObjectiveIt has been recognized that there is a nexus among Trisomy 8 (T8), Behcet's disease (BD), and myelodysplastic syndrome (MDS). We reported a series of inflammatory features in 2 children with T8 without hematological involvement.Methods2 chil
Externí odkaz:
https://doaj.org/article/7e751300efd04b1aa9b98c706fdf48a3
Autor:
Lin Liu, Jinghan Wang, Huan Xu, Shuqi Zhao, Lu Wang, Jiansong Huang, Huanping Wang, Hongyan Tong, Jie Jin
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
ABSTRACTObjectives In patients with acute promyelocytic leukemia (APL), additional chromosomal abnormalities (ACAs) are prognostic indicators. However, the clinical features of ACAs were not systematically reported in Chinese patients. Therefore, we
Externí odkaz:
https://doaj.org/article/7241f6f5a9d74c6194fce1f0acd6f5c1
Autor:
Ryo Takahashi, Yasuo Matsubara, Satoshi Takahashi, Kazuaki Yokoyama, Lim Lay Ahyoung, Michiko Koga, Hiroyuki Sakamoto, Narikazu Boku, Dai Shida, Hiroshi Yotsuyanagi
Publikováno v:
Case Reports in Gastroenterology, Vol 17, Iss 1, Pp 287-293 (2023)
Intestinal Behçet disease (BD), associated with myelodysplastic syndrome (MDS), is often refractory to treatment. An 80-year-old man with trisomy 8 MDS (refractory anemia) developed intermittent fever. Despite investigations to exclude infectious di
Externí odkaz:
https://doaj.org/article/26c0aa44a26a4b27b800adf9e58a5ff4
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTObjective This study aims to construct a nomogram model for predicting poor prognosis in acute leukemia with trisomy 8.Methods A retrospective analysis was conducted on 244 patients with primary acute leukemia with trisomy 8 who received trea
Externí odkaz:
https://doaj.org/article/dbe9c55a9f9e4740a1707352ec6d11c4
Publikováno v:
Xiehe Yixue Zazhi, Vol 14, Iss 2, Pp 299-305 (2023)
Objective The clinical characteristics of children with Behçet's disease like trisomy 8 (T8-BD) diagnosed and treated in multi-centers were summarized, so as to improve the understanding and treatment ability of clinicians. Methods Clinical data of
Externí odkaz:
https://doaj.org/article/5b05c88c3d8b400b86173e7319915bea
Autor:
Jie Liu, WenMin Han, Xiaohui Cai, Zheng Wang, LiuJun Cao, HaiYing Hua, ZhuXia Jia, HongYing Chao, XuZhang Lu, HongJie Shen
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 565-574 (2022)
Introduction The aim of the study was to determine molecular genetic and clinical characterization of acute myeloid leukemia (AML) with trisomy 8 as the sole chromosome abnormality, a recurrent but rare chromosomal abnormality in AML.Methods Interpha
Externí odkaz:
https://doaj.org/article/c00a530fdb5e4b46a9b10420fb134e27
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-7 (2022)
Abstract Background So called cell-free fetal DNA (cffDNA) in the maternal plasma, which is derived from placenta, is widely used to screen fetal aneuploidies, including trisomy 21, 18, 13 and sex chromosomes. Here we reported a case of trisomy 8 mos
Externí odkaz:
https://doaj.org/article/53e1be581e0645c9b100baaf1cffce60
Autor:
Sofía Toribio-Castelló, Sandra Castaño, Ángela Villaverde-Ramiro, Esperanza Such, Montserrat Arnán, Francesc Solé, Marina Díaz-Beyá, María Díez-Campelo, Mónica del Rey, Teresa González, Jesús María Hernández-Rivas
Publikováno v:
Cancers, Vol 15, Iss 15, p 3822 (2023)
Trisomy 8 (+8) is the most frequent trisomy in myelodysplastic syndromes (MDS) and is associated with clinical heterogeneity and intermediate cytogenetic risk when found in isolation. The presence of gene mutations in this group of patients and the p
Externí odkaz:
https://doaj.org/article/82d7b36ecb6742e6aade89bfbfcb4919
Autor:
Hiroshi Shimizu, Shuzo Sato, Tomohiro Suzuki, Tomomi Sasajima, Yosuke Takahata, Nobuhiko Shinohara, Kosuke Hideshima, Yuko Yokokawa, Nobuo Matsuhashi, Osamu Ichii, Mayumi Tai, Yutaka Ejiri, Kiori Yano, Takayuki Ikezoe, Hiromasa Ohira, Kiyoshi Migita
Publikováno v:
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Gastrointestinal lesions, which sometimes develop in Behçet’s disease (BD), are referred to as intestinal BD. Although rare, intestinal BD can be accompanied by myelodysplastic syndrome (MDS) with abnormal karyotype trisomy 8,
Externí odkaz:
https://doaj.org/article/3ba95f267faa4028ba1bb8c914e2b261
Autor:
Xiaofen Zhang, Meng Jin, Zhe Shen, Xingyong Wan, Lan Li, Yuwei Zhang, Xinping Zhou, Chen Mei, Hongyan Tong, Chaohui Yu
Publikováno v:
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Trisomy 8 positivity myelodysplastic syndrome with Behçet's disease is rare. Isolated trisomy 8 is a frequent cytogenetic abnormality in the MDS, but the characteristic of trisomy 8 and the association between trisomy 8 positivit
Externí odkaz:
https://doaj.org/article/41acb89938ef4087971f01b8c012d6ff