Hematolojik Kanser Tanılı Hastaların Kemik İliği Örneklerindeki Kromozomal Anomaliler: Tek Merkezden 109 Olgunun FISH Sonuçları
نویسندگان
چکیده
Objective: Hematological cancers are a group of neoplasms that affect the bone marrow, blood and lymph nodes, usually associated with structural numerical chromosomal abnormalities. Bone marrow examination in hematological has an illuminating guiding role diagnosis prognosis disease. In our study, it was aimed to retrospectively evaluate results obtained by using Fluorescent Situ Hybridization (FISH) method certain genetic disorders patients cancer. Materials & Methods: between January 1, 2021 November 30, The from samples 109 (KML n=14, AML n=40, KLL n=6, ALL n=27, M.Myelom n=22) pre-diagnosis cancer, who were referred Dicle University Faculty Medicine, Department Medical Biology Genetics, Hematology other clinics, analyzed terms age, gender, disease distribution. All included study evaluated anomalies, changes, or presence balanced translocation. Results: There 47 female 62 male patients, mean age 48±21.6 years. As result cases, known for AML; t(15;17), monosomy 7 trisomy 8, t(9;22) KML; del(13q14) del(17p13) KLL, t(11;14)(q13;q32) M. Myeloma, (t[9;22]) (bcr-abl) t(4;11) chromosome changes such as shown first. addition, comparison groups, no significant difference found materials participating female. Conclusion: this which we conducted prediagnosed cancer FISH method, regarding prognostically important anomalies diseases. Rapid accurate diseases is very treatment planning course result, considering difficulty obtaining cells taken under limited difficult conditions according results, concluded powerful effective technique used genetics, since provides opportunity work even interphase cells.
منابع مشابه
Platelet-to-lymphocyte Ratio in Diagnosis of Acute Complicated Appendicitis in Childhood Çocukluk Çaği Akut Kompli̇ke Apandi̇si̇t Tanisinda Platelet Lenfosi̇t Orani
DOI: 10.4328/JCAM.4873 Received: 27.11.2016 Accepted: 20.12.2016 Printed: 01.07.2017 J Clin Anal Med 2017;8(4): 299-301 Corresponding Author: Mervan Bekdas, Department of Pediatrics, Abant Izzet Baysal University Faculty of Medicine, Bolu, Turkey. E-Mail: [email protected] Öz Amaç: Akut komplike apandisit tanısının geç veya yanlış konulması morbidite ve mortaliteyi arttırabilmektedir. Bu çalış...
متن کاملTavuklarda Kemik Morfogenetik Protein Reseptörü 1B (BMPR-1B) Genindeki Tek Nükleotid Polimorfizmi ile Büyüme Özellikleri Arasındaki İlişki
Growth traits are under the control of multiple genes. Understanding the genetic information of related genes is helpful for the selection and breeding course through marker assisted selection. The aim of the current study was to investigate the association of A287G SNP in BMPR-1B gene with growth traits in chicken. A single nucleotide polymorphism was identified in 240 individuals using the PC...
متن کاملThe TEK
The Internet has the potential to deliver information to areas of the world that have no other information resources. High telephone and ISP fees – in combination with low bandwidth connections – make it unaffordable for many people to browse the Web online. We are developing the TEK system to enable users to search the Web using only email. TEK stands for “Time Equals Knowledge,” since the use...
متن کاملAssessment of Cardiovascular Risks due to Methylphenidate in Six Months of Treatment in Children with Attention Deficit and Hyperactivity Disorder
Amaç: Dikkat eksikliği ve hiperaktivite bozukluğu (DEHB) nedeniyle metilfenidat kullanan hastalarda nadiren kardiyovasküler yan etkiler görülebilmektedir. Bu çalışmada, DEHB’li hastalarda metilfenidatın kardiovasküler sistem üzerine etkilerininin araştırılması planlandı. Yöntem: Mayıs 2011-Mayıs 2012 tarihleri arasında DEHB tanısı ile metilfenidat tedavisi başlanan 141 hasta incelendi. Hastalar...
متن کاملRare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases Prenatal Tanıda Nadir Yapısal Kromozom Anomaliler; 10125 Prenatal Olgunun Klinik ve Sitogenetik Bulguları
Results: A structural chromosomal abnormality was observed in 95 cases. The most frequently observed structural abnormalities were balanced translocations with a frequency of 53.7% (51 cases) followed by unbalanced translocations (16.8%), inversions (11.6%), supernumerary marker chromosomes (8.4%), duplications (4.2%), deletions and ring chromosomes (2.1%) and complex translocation (1.1%). rare...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Ege t?p bilimleri dergisi
سال: 2022
ISSN: ['2636-851X']
DOI: https://doi.org/10.33713/egetbd.1118486