The 5q – syndrome: an underdiagnosed form of macrocytic anaemia
- 1 May 1983
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 54 (1) , 103-110
- https://doi.org/10.1111/j.1365-2141.1983.tb02072.x
Abstract
Since the description in 1974 of the 5q- syndrome, only 29 cases have been reported. Over a 3.5 yr period cytogenetic culture of bone marrow submitted from 344 patients being investigated for a blood disorder revealed 9 patients with anomalies of chromosome 5. In 5 of these patients (samples arising from 37 patients being investigated for refractory macrocytic or aplastic anemia) the 5q- syndrome was diagnosed. The clinical and hematological findings of this syndrome are reviewed and attention is drawn to the importance of reviewing megakaryocytic numbers and morphology in refractory macrocytic anemia if the diagnosis is to be considered. The diagnosis is compatible with prolonged survival and establishing it prevents repeated and unnecessary investigation.This publication has 15 references indexed in Scilit:
- Clustering of aberrations to specific chromosomes in human neoplasmsHereditas, 2009
- Proposals for the classification of the myelodysplastic syndromesBritish Journal of Haematology, 1982
- 5q- syndrome in a patient with chronic exposure to ionizing radiationCancer Genetics and Cytogenetics, 1982
- The 5q- chromosome in a case of erythroid hypoplasiaCancer Genetics and Cytogenetics, 1981
- Simultaneous occurrence of 5q− and 21q− in refractory anemia with thrombocytosisCancer Genetics and Cytogenetics, 1979
- Chromosomes and causation of human cancer and leukemia. XXXIII. 5q– in a case of acute lymphoblastic leukemia (ALL)American Journal of Hematology, 1979
- The preleukemic syndrome (hemopoietic dysplasia)Cancer, 1978
- Continuous Subcutaneous Administration of Deferoxamine in Patients with Iron OverloadNew England Journal of Medicine, 1977
- Proposals for the Classification of the Acute Leukaemias French‐American‐British (FAB) Co‐operative GroupBritish Journal of Haematology, 1976
- Distinct haematological disorder with deletion of long arm of No. 5 chromosomeNature, 1974