Literature DB >> 21686867

Rieger syndrome with multiple chromosomal breaks and chromosome 4 deletion.

Mukesh Tanwar1, Rakesh Kumar, Amita Goyal, Manoj Kumar, Tanuj Dada, Gurdeep Singh, Ramanjit Sihota, Rima Dada.   

Abstract

Rieger syndrome (RS) is a rare autosomal dominant disorder with variable expressivity and complete penetrance. Axenfeld-Rieger syndrome (ARS) shows genetic heterogeneity with mutations in several chromosomal loci being implicated including PITX2, FOXC1 and PAX6. Cytogenetic analysis was done in this case. Patient had de novo 46,XY,del(4q25-q27) karyotype with a high percentage (>35%) of chromosomal breaks. The breaks were on different chromosomes and not related to disease phenotype of RS. Such chromosomal breaks are diagnostic of chromosomal instability syndromes. Available literature does not report chromosomal breaks in RS or due to culture condition. Such a high percentage of chromosomal breaks are associated with development of certain cancers. In the present case we did not find any features consistent with any of the chromosomal instability syndromes like Fanconi's anaemia and Blooms syndrome, but such cases need to be under regular follow-up. Thus RS cases with multiple chromosomal breaks need regular follow-up and genetic counselling.

Entities:  

Year:  2009        PMID: 21686867      PMCID: PMC3029512          DOI: 10.1136/bcr.06.2008.0297

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  11 in total

1.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

2.  A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome.

Authors:  Brian P Brooks; Sayoko E Moroi; Catherine A Downs; Shannon Wiltse; Mohammad I Othman; Elena V Semina; Julia E Richards
Journal:  Ophthalmic Genet       Date:  2004-03       Impact factor: 1.803

Review 3.  Current molecular understanding of Axenfeld-Rieger syndrome.

Authors:  Tord A Hjalt; Elena V Semina
Journal:  Expert Rev Mol Med       Date:  2005-11-08       Impact factor: 5.600

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Authors:  R J Jorgenson; L S Levin; H E Cross; F Yoder; T E Kelly
Journal:  Am J Med Genet       Date:  1978

5.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321

6.  PITX genes are required for cell survival and Lhx3 activation.

Authors:  Michael A Charles; Hoonkyo Suh; Tord A Hjalt; Jacques Drouin; Sally A Camper; Philip J Gage
Journal:  Mol Endocrinol       Date:  2005-03-10

7.  The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability.

Authors:  Niall G Howlett; Toshiyasu Taniguchi; Sandra G Durkin; Alan D D'Andrea; Thomas W Glover
Journal:  Hum Mol Genet       Date:  2005-01-20       Impact factor: 6.150

8.  Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.

Authors:  F Mirzayans; D B Gould; E Héon; G D Billingsley; J C Cheung; A J Mears; M A Walter
Journal:  Eur J Hum Genet       Date:  2000-01       Impact factor: 4.246

9.  Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.

Authors:  E V Semina; R Reiter; N J Leysens; W L Alward; K W Small; N A Datson; J Siegel-Bartelt; D Bierke-Nelson; P Bitoun; B U Zabel; J C Carey; J C Murray
Journal:  Nat Genet       Date:  1996-12       Impact factor: 38.330

Review 10.  Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).

Authors:  Y Makita; M Masuno; K Imaizumi; S Yamashita; S Ohba; D Ito; Y Kuroki
Journal:  Am J Med Genet       Date:  1995-05-22
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