Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns
- PMID: 3879440
Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns
Abstract
In the present paper we report a characteristic pattern of external and internal malformations in two male siblings with proximal 7q interstitial deletion as the unbalanced product of a rearranged chromosome 7 in the mother with karyotype 47,XX,del(7)(pter----cen::q21----qter),+fr. The interstitial 7q deletion in the mother included centromeric fission, break at 7q21 and preservation of the proximal q arm fragment.
Similar articles
-
Proximal interstitial deletion of 7q: a case report and review of the literature.Am J Med Genet. 1990 Jul;36(3):328-32. doi: 10.1002/ajmg.1320360317. Am J Med Genet. 1990. PMID: 2194394 Review.
-
Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.Ann Genet. 1990;33(1):43-5. Ann Genet. 1990. PMID: 2195980 Review.
-
Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.Ann Genet. 1989;32(1):59-61. Ann Genet. 1989. PMID: 2751251
-
Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.Ann Genet. 1982;25(3):141-4. Ann Genet. 1982. PMID: 6982660
-
Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen.Am J Med Genet. 1996 Oct 2;65(1):56-9. doi: 10.1002/(SICI)1096-8628(19961002)65:1<56::AID-AJMG9>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8914742
Cited by
-
Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.Am J Hum Genet. 2008 Feb;82(2):398-410. doi: 10.1016/j.ajhg.2007.10.013. Am J Hum Genet. 2008. PMID: 18252220 Free PMC article.
-
Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier.Mol Cytogenet. 2009 Jan 23;2:3. doi: 10.1186/1755-8166-2-3. Mol Cytogenet. 2009. PMID: 19166580 Free PMC article.
-
Interstitial deletion of proximal 8q including part of the centromere from unbalanced segregation of a paternal deletion/marker karyotype with neocentromere formation at 8p22.Cytogenet Genome Res. 2011;132(4):227-32. doi: 10.1159/000322815. Epub 2011 Jan 6. Cytogenet Genome Res. 2011. PMID: 21212645 Free PMC article.
-
Centric fission--simple and complex mechanisms.Chromosome Res. 2004;12(6):627-40. doi: 10.1023/B:CHRO.0000036594.38997.59. Chromosome Res. 2004. PMID: 15289668 Review.
-
A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.J Med Genet. 1989 Oct;26(10):619-25. doi: 10.1136/jmg.26.10.619. J Med Genet. 1989. PMID: 2486209 Free PMC article.