Translocation 4p;21q identified by FISH in a case previously described as "presumptive monosomy 21"

Recently, Lopez-Pajares et al. (1993) reported identification of a translocation between the short arm of a chromosome 5 and the long arm of a chromosome 21 in a patient who was thought to be monosomy 21. This study is the first application of a chromosome 21 painting probe, pBS-21, and fluorescent...

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Veröffentlicht in:American Journal of Medical Genetics 1994-10, Vol.52 (4), p.491-492
Hauptverfasser: Yao, Xiu-Lan, Jenkins, Edmund C.
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container_title American Journal of Medical Genetics
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creator Yao, Xiu-Lan
Jenkins, Edmund C.
description Recently, Lopez-Pajares et al. (1993) reported identification of a translocation between the short arm of a chromosome 5 and the long arm of a chromosome 21 in a patient who was thought to be monosomy 21. This study is the first application of a chromosome 21 painting probe, pBS-21, and fluorescent in situ chromosome hybridization (FISH) to revise an earlier diagnosis of monosomy 21. We have now restudied skin fibroblast cultures, GM00137B, that are still available from another patient previously described as {open_quotes}presumptive monosomy 21{close_quotes} and have found that this case also has a translocation involving chromosomes 21 and 4. The authors urge that all previous cases of what appeared to be monosomy 21 should be re-examined with FISH to confirm or revise the original diagnosis so that genetic counseling of the family may be updated. 3 refs., 3 figs.
doi_str_mv 10.1002/ajmg.1320520418
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identifier ISSN: 0148-7299
ispartof American Journal of Medical Genetics, 1994-10, Vol.52 (4), p.491-492
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source MEDLINE; Alma/SFX Local Collection
subjects ACCURACY
BIOLOGY AND MEDICINE, BASIC STUDIES
CHROMOSOMAL ABERRATIONS
Chromosome Deletion
Chromosomes, Human, Pair 21
Diagnostic Errors
DIAGNOSTIC TECHNIQUES
DNA HYBRIDIZATION
FLUORESCENCE
GENES
HUMAN CHROMOSOME 21
Humans
In Situ Hybridization, Fluorescence
Monosomy - diagnosis
PHENOTYPE
Translocation, Genetic
title Translocation 4p;21q identified by FISH in a case previously described as "presumptive monosomy 21"
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