Literature DB >> 8733051

Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH.

E Blennow1, E Tillberg.   

Abstract

We present a case with a small extra ring chromosome which was found in 66% of lymphocytes on routine cytogenetic examination. FISH analyses, using centromere specific and single copy probes, showed that the extra ring chromosome was derived from the most proximal part of 10p, close to the centromere. The patient has a unilateral cleft lip and palate, mild dysmorphic features, and mild mental retardation. Only a limited number of extra ring chromosomes have been characterised so far. To our knowledge, this is the first reported patient with an extra ring chromosome derived from chromosome 10p.

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Year:  1996        PMID: 8733051      PMCID: PMC1050610          DOI: 10.1136/jmg.33.5.399

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  26 in total

1.  Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

Authors:  D F Callen; H J Eyre; M L Ringenbergs; C J Freemantle; P Woodroffe; E A Haan
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

2.  Extra marker chromosome in newborn children.

Authors:  J Nielsen; K Rasmussen
Journal:  Hereditas       Date:  1975       Impact factor: 3.271

3.  Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age.

Authors:  E B Hook; P K Cross
Journal:  Am J Hum Genet       Date:  1987-02       Impact factor: 11.025

4.  A cytogenetic survey of 11,680 newborn infants.

Authors:  P A Jacobs; M Melville; S Ratcliffe; A J Keay; J Syme
Journal:  Ann Hum Genet       Date:  1974-05       Impact factor: 1.670

5.  Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses.

Authors:  M A Ferguson-Smith; J R Yates
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

6.  Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis.

Authors:  D Warburton
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

7.  A small supernumerary marker chromosome X identified by in situ hybridization.

Authors:  A N Silahtaroglu; S Hacihanefioglu; S Yilmaz; Y Tarkan; A Cenani; Z Tümer
Journal:  Clin Genet       Date:  1995-05       Impact factor: 4.438

8.  Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

Authors:  D F Callen; M L Ringenbergs; J C Fowler; C J Freemantle; E A Haan
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318

9.  A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

Authors:  J L Hamerton; N Canning; M Ray; S Smith
Journal:  Clin Genet       Date:  1975-10       Impact factor: 4.438

10.  Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Authors:  Y Y Fang; H J Eyre; S K Bohlander; A Estop; E McPherson; T Träger; O Riess; D F Callen
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

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  4 in total

Review 1.  Reverse painting highlights the origin of chromosome aberrations.

Authors:  Elisabeth Blennow
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

2.  Neurophysiological findings in a newborn with chromosome 10 trisomy.

Authors:  Simone Vidale; Franco Di Palma; Luigi Sironi; Marco Arnaboldi
Journal:  BMJ Case Rep       Date:  2014-05-05

3.  Further studies on a male monozygotic triplet with schizophrenia: cytogenetical and neurobiological assessments in the patients and their parents.

Authors:  E G Jönsson; C Härnryd; T Johannesson; J Wahlström; J Bergenius; H Bergstedt; D Greitz; H Nyman; E Björck; E Blennow; G C Sedvall
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1997       Impact factor: 5.270

4.  Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling.

Authors:  Margaret E Armstrong; David D Weaver; Melissa D Lah; Gail H Vance; Benjamin J Landis; Stephanie M Ware; Benjamin M Helm
Journal:  Mol Cytogenet       Date:  2018-03-27       Impact factor: 2.009

  4 in total

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