A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH‐technique
- 28 June 1996
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 49 (6) , 303-305
- https://doi.org/10.1111/j.1399-0004.1996.tb03793.x
Abstract
We report a new chromosomal finding in a 20 month-old girl. The minor clinical features included: moderate mental retardation, microcephaly, mild hypotonia and hypertelorism. Initially, what appeared to be a terminal deletion of the long arm of one chromosome 15 [15q26-->qter] was determined to be an interstitial deletion involving band 15q25 as revealed by FISH-technique, showing the presence of intact telomeric hybridization signals. The cytogenetic diagnosis was thus modified to 46,XX, del (15) (pter-->q24::q26--> qter). Nevertheless, the function of the enzyme telomerase should not be ignored, as healing could occur following such terminal deletions. Consequently, it will remain a difficult task to distinguish terminal deletions from those that are interstitial.Keywords
This publication has 8 references indexed in Scilit:
- Telomeric and Nontelomeric (TTAGGG)n Sequences in Gene Amplification and Chromosome StabilityGenomics, 1994
- Telomere capture stabilizes chromosome breakageNature Genetics, 1993
- Telomeres and their possible role in chromosome stabilizationEnvironmental and Molecular Mutagenesis, 1993
- Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysisHuman Molecular Genetics, 1992
- A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.Journal of Medical Genetics, 1990
- Interstitial deletion of chromosome 15: two casesHuman Genetics, 1988
- Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.Journal of Medical Genetics, 1987