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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1992 Oct;29(10):742–744. doi: 10.1136/jmg.29.10.742

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

L R Willatt 1, B C Davison 1, D Goudie 1, J Alexander 1, H M Dyson 1, P E Jenks 1, M E Ferguson-Smith 1
PMCID: PMC1016137  PMID: 1433238

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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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Diaz-Mares L., Molina B., Carnevale A. Trisomy 9 mosaicism in a girl with multiple malformations. Ann Genet. 1990;33(3):165–168. [PubMed] [Google Scholar]
  2. Frydman M., Shabtal F., Halbrecht I., Elian E. Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9. J Med Genet. 1981 Oct;18(5):390–392. doi: 10.1136/jmg.18.5.390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Schinzel A., Hayashi K., Schmid W. Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy. Humangenetik. 1974;25(3):171–177. doi: 10.1007/BF00281424. [DOI] [PubMed] [Google Scholar]
  4. Temple I. K., Cockwell A., Hassold T., Pettay D., Jacobs P. Maternal uniparental disomy for chromosome 14. J Med Genet. 1991 Aug;28(8):511–514. doi: 10.1136/jmg.28.8.511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Warburton D. Uniparental disomy: a rare consequence of the high rate of aneuploidy in human gametes. Am J Hum Genet. 1988 Feb;42(2):215–216. [PMC free article] [PubMed] [Google Scholar]

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