13q-/r(13) mosaicism
- PMID: 7205909
- PMCID: PMC1048579
- DOI: 10.1136/jmg.17.4.316
13q-/r(13) mosaicism
Abstract
A 2-month-old female infant with typical features of the 13q-syndrome was found to be a hitherto unreported mosaic consisting of 46,XX,del(13)(q22)-46,XX,r(13)(p13q22). Both of the 13q- and r(13) chromosomes were Ag N banding positive. Therefore, it was assumed that they had retained the satellite stalks. Two possible mechanisms were proposed for the genesis of the mosaicism. Firstly, the patients started with the 13q- chromosome, which then underwent breakage and reunion at both ends to form the r(13) chromosome. Secondly, the patients started with the r(13) chromosome, which reopened at or close to the joining point to form the 13q- chromosome.
Similar articles
-
[Ring chromosome 13 and multiple malformations (author's transl)].An Esp Pediatr. 1981 Nov;15(5):469-73. An Esp Pediatr. 1981. PMID: 7332149 Spanish.
-
13q-/r(13) mosaicism.Eur J Pediatr. 1981 Mar;136(1):101-4. doi: 10.1007/BF00441721. Eur J Pediatr. 1981. PMID: 7215384
-
Dicentric chromosome 13 and centromere inactivation.Hum Genet. 1983;63(4):332-7. doi: 10.1007/BF00274757. Hum Genet. 1983. PMID: 6862437
-
Mosaic tetrasomy 8p.Am J Med Genet. 1993 Jun 15;46(5):513-6. doi: 10.1002/ajmg.1320460510. Am J Med Genet. 1993. PMID: 8322811 Review.
-
Mosaic isochromosome 8p.Am J Med Genet. 1993 Jun 15;46(5):517-9. doi: 10.1002/ajmg.1320460511. Am J Med Genet. 1993. PMID: 8322812 Review.
Cited by
-
Distribution of break points in human structural rearrangements.Am J Hum Genet. 1983 Mar;35(2):288-300. Am J Hum Genet. 1983. PMID: 6340471 Free PMC article. Review.
-
High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19.Hum Genet. 1993 Mar;91(1):42-4. doi: 10.1007/BF00230220. Hum Genet. 1993. PMID: 8454286
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources