Introduction. Among patients with Acute Myeloid Leukemia (AML), the karyotype at diagnosis is an important prognostic indicator for predicting outcomes. Several studies have been done to identify most common cytogenetic abnormalities seen in other countries, however, limited our setting. Objective. The study aims determine present among AML referred Fluorescence situ Hybridization (FISH) Nation...

Introduction Turner syndrome characterized by total/partial and/or homogeneous/mosaic X chromosome monosomy is associated with various physical health concerns, including facial dysmorphism, short stature, infertility, and other organ defects such as heart, kidney, bone, skin, … well variable degrees of cognitive impairments. Besides, social skills, communication relationships are usually disor...

Myeloid/lymphoid neoplasms with FGFR1 rearrangement (MLN-FGFR1) comprise a heterogeneous group of that can present as myeloproliferative neoplasm, myelodysplastic/myeloproliferative acute myeloid leukemia, T or B lymphoblastic leukemia/lymphoma, mixed phenotype leukemia. The overall outcome these is poor, and patients often show cytogenetic evolution gain additional chromosomal abnormalities le...

Consistent chromosomal abnormalities have been described in several leukemic disorders, but relatively little is known about the cytogenetic features of juvenile chronic myelogenous leukemia (JCML). We report the serial cytogenetic findings over a 2-yr period for a patient with JCML. A large subtelocentric marker chromosome was noted in all metaphases throughout the course of his disease and pr...