Literature DB >> 1433238

A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line.

L R Willatt1, B C Davison, D Goudie, J Alexander, H M Dyson, P E Jenks, M E Ferguson-Smith.   

Abstract

We describe a 17 year old male with a low level of trisomy 9 mosaicism. Maternal uniparental chromosome 9 disomy in the euploid cell line was shown to have arisen after postzygotic loss of the paternal chromosome 9 from the trisomic cell line by cytogenetic and molecular analysis. This is believed to be the first report of uniparental disomy for chromosome 9. In four of the 11 reported cases of mosaic trisomy 9 syndrome, including our patient, a maternally derived pericentric inversion of the heterochromatic area of chromosome 9 has been present in duplicate in the trisomic cell line. This may have implications for the counselling of patients with this common chromosomal variant.

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Year:  1992        PMID: 1433238      PMCID: PMC1016137          DOI: 10.1136/jmg.29.10.742

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


  5 in total

Review 1.  Trisomy 9 mosaicism in a girl with multiple malformations.

Authors:  L Diaz-Mares; B Molina; A Carnevale
Journal:  Ann Genet       Date:  1990

2.  Uniparental disomy: a rare consequence of the high rate of aneuploidy in human gametes.

Authors:  D Warburton
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

3.  Maternal uniparental disomy for chromosome 14.

Authors:  I K Temple; A Cockwell; T Hassold; D Pettay; P Jacobs
Journal:  J Med Genet       Date:  1991-08       Impact factor: 6.318

4.  Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1974

5.  Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9.

Authors:  M Frydman; F Shabtal; I Halbrecht; E Elian
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

  5 in total
  2 in total

1.  Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.

Authors:  K Devriendt; G Matthijs; S Claes; E Legius; W Proesmans; J J Cassiman; J P Fryns
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.

Authors:  L M Brzustowicz; B A Allitto; D Matseoane; R Theve; L Michaud; S Chatkupt; E Sugarman; G K Penchaszadeh; L Suslak; M R Koenigsberger
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

  2 in total

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