91桃色

Journal of Oncology Research and Treatment
Open 91桃色

Our Group organises 3000+ Global Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open 91桃色 Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open 91桃色 Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Cytogenetic Features of Patients with de novo Acute Myeloid Leukemia in Kurdistan Region of Iraq

Ch Satish Kumar and Navnit Basnet*
*Corresponding Author: Navnit Basnet, Department of Public Health, SRM University, India, Email: navnitr_basnet@srmus.edu.in

Received Date: Nov 17, 2023 / Published Date: Jan 22, 2025

Citation: Hamad GH (2025) Cytogenetic Features of Patients with de novo Acute Myeloid Leukemia in Kurdistan Region of Iraq. J Oncol Res Treat 10: 309.

Copyright: © 2025 Hamad GH. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

 
To read the full article Peer-reviewed Article PDF image

Abstract

Background: AML is a complex condition marked by the growth of immature cells of the myeloid origin. There is currently minimal data on the mutational spectrum of AML patients in Kurdistan Region of Iraq.

Methods: Samples from peripheral blood and bone marrow were collected from 100 AML patients and used for cytogenetic analysis. Fluorescence in situ Hybridization (FISH) using probes for detection of 5q, 7q, 3q, t(9;11), t(8;21), 11q23, t(6;11), t(15;17), and inv(16) chromosomal abnormalities for disease risk-stratification and classify AML.

Results: The median age was 37 with AML-M2 makes up 43% of all cases. Chromosomal aberrations were observed in 48% of patients. The most prevalent structural abnormality was t(8;21) in 14% of patients, followed by inv(16), t(15;17), 11q23 translocations, and inv(3) in 7% and 5%, and 3% and 2% respectively. In terms of numerical abnormalities, +8 was found in 7% of cases followed by loss of sex chromosomes (6%), +11 (3%), +21 (2%), and each -7/del(7q) and -5/del (5q) in 1%. Additional chromosomal abnormalities commonly found with t(8;21), t(15;17) and inv(16) were present in 12%, 4% and 4% of cases consequently. 28% of patients were classified as having favorable risk, 64% as having intermediate risk, and 8% as having adverse risk.

Conclusion: Here we provide the initial presentation of a cytogenetic profile of Kurdistan Region of Iraqi individuals who have newly developed AML. Findings can help in accurate diagnostic and improves accuracy of risk assessment and facilitates the use of therapy choices.

Keywords

International Conferences 2025-26
 
Meet Inspiring Speakers and Experts at our 3000+ Global

Conferences by Country

Medical & Clinical Conferences

Conferences By Subject

Top