Interstitial del(12)(q15q22) in myelodysplastic syndromes

M T Ferro; J M García-Sagredo; M Resino; J Laraña; E Cabezudo; C San Román

doi:10.1016/0165-4608(94)00181-a

Interstitial del(12)(q15q22) in myelodysplastic syndromes

Cancer Genet Cytogenet. 1995 Apr;80(2):158-9. doi: 10.1016/0165-4608(94)00181-a.

Authors

M T Ferro¹, J M García-Sagredo, M Resino, J Laraña, E Cabezudo, C San Román

Affiliation

¹ Medical Genetics Department, Hospital Ramón y Cajal, Madrid, Spain.

PMID: 7736435
DOI: 10.1016/0165-4608(94)00181-a

Abstract

A patient with a myelodysplastic syndrome and a 12q deletion was studied and followed-up. After 10 years and several cytogenetic studies, it is suggested that this abnormality can be the sole chromosomal change in myelodysplastic syndromes.

Publication types

Case Reports

MeSH terms

Anemia, Refractory, with Excess of Blasts / genetics*
Chromosome Deletion*
Chromosomes, Human, Pair 12*
Female
Humans
Middle Aged