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. 1989 Jan;26(1):58–60. doi: 10.1136/jmg.26.1.58

A case of interstitial deletion of 10q25.2----q26.1.

D E Rooney 1, K Williams 1, D V Coleman 1, A Habel 1
PMCID: PMC1015539  PMID: 2918528

Abstract

A de novo interstitial deletion of chromosome 10, del(10)(pter----q25.2::q26.1----qter), was detected in a newborn female with facial anomalies, failure to thrive, and subsequent developmental delay. This case is compared with 10 previous reports of monosomy 10q within the q25----qter region.

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Selected References

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  1. Brusnický J., van Heerden K. M., de Jong G., Cronjé A. S., Retief A. E. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2). J Med Genet. 1986 Oct;23(5):435–445. doi: 10.1136/jmg.23.5.435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chieri P., Iölster N. Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23). Clin Genet. 1983 Aug;24(2):147–150. doi: 10.1111/j.1399-0004.1983.tb02226.x. [DOI] [PubMed] [Google Scholar]
  3. Curtis H., Howell R. T., Cope C. Terminal deletion of the long arm of chromosome 10. J Med Genet. 1986 Oct;23(5):478–480. doi: 10.1136/jmg.23.5.478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Evans-Jones G., Walker S., Howard P. J. A further case of monosomy 10qter. Clin Genet. 1983 Sep;24(3):216–219. doi: 10.1111/j.1399-0004.1983.tb02242.x. [DOI] [PubMed] [Google Scholar]
  5. Junien C., Despoisse S., Turleau C., de Grouchy J., Bucher T., Fundele R. Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3). Ann Genet. 1982;25(1):25–27. [PubMed] [Google Scholar]
  6. Lewandowski R. C., Jr, Kukolich M. K., Sears J. W., Mankinen C. B. Partial deletion 10q. Hum Genet. 1978 Jun 27;42(3):339–343. doi: 10.1007/BF00291317. [DOI] [PubMed] [Google Scholar]
  7. Mehta L., Duckett D. P., Young I. D. Behaviour disorder in monosomy 10qter. J Med Genet. 1987 Mar;24(3):185–186. doi: 10.1136/jmg.24.3.185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mulcahy M. T., Pemberton P. J., Thompson E., Watson M. Is there a monosomy 10qter syndrome? Clin Genet. 1982 Jan;21(1):33–35. doi: 10.1111/j.1399-0004.1982.tb02076.x. [DOI] [PubMed] [Google Scholar]
  9. Shapiro S. D., Hansen K. L., Pasztor L. M., DiLiberti J. H., Jorgenson R. J., Young R. S., Moore C. M. Deletions of the long arm of chromosome 10. Am J Med Genet. 1985 Jan;20(1):181–196. doi: 10.1002/ajmg.1320200122. [DOI] [PubMed] [Google Scholar]
  10. Taysi K., Strauss A. W., Yang V., Padmalatha C., Marshall R. E. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature. Ann Genet. 1982;25(3):141–144. [PubMed] [Google Scholar]
  11. Turleau C., de Grouchy J., Ponsot G., Bouygues D. Monosomy 10qter. Hum Genet. 1979 Apr 5;47(3):233–237. doi: 10.1007/BF00321014. [DOI] [PubMed] [Google Scholar]
  12. Vanlieferinghen P., Dechelotte P., Charbonné F. Délétion partielle 10qter. Une nouvelle observation. Ann Genet. 1987;30(2):118–121. [PubMed] [Google Scholar]
  13. Wegner R. D., Kunze J., Paust H. Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24). Clin Genet. 1981 Feb;19(2):130–133. doi: 10.1111/j.1399-0004.1981.tb00683.x. [DOI] [PubMed] [Google Scholar]
  14. Zatterale A., Pagano L., Fioretti G., Caniglia M., Festa B., Renda S., Rinaldi M. M., Ventruto V. Clinical features of monosomy 10qter. Ann Genet. 1983;26(2):106–108. [PubMed] [Google Scholar]

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