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. 1988 Apr;25(4):260–262. doi: 10.1136/jmg.25.4.260

De novo partial trisomy 15q (proximal type).

T J Herweijer 1, J W Oorthuys 1, N J Leschot 1
PMCID: PMC1015510  PMID: 2966860

Abstract

This report describes a retarded girl with strabismus, high arched palate, antimongoloid slant, low set ears, hearing loss, micrognathia, short neck, and an anteriorly displaced anus. She was found to have a de novo partial trisomy of the proximal part of the long arm of chromosome 15.

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Selected References

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

  1. Annerén G., Gustavson K. H. A boy with proximal trisomy 15 and a male foetus with distal trisomy 15 due to a familial 13p;15q translocation. Clin Genet. 1982 Jul;22(1):16–21. doi: 10.1111/j.1399-0004.1982.tb01404.x. [DOI] [PubMed] [Google Scholar]
  2. Bannister D. L., Engel E. A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange. J Pediatr. 1975 Jun;86(6):916–917. doi: 10.1016/s0022-3476(75)80228-9. [DOI] [PubMed] [Google Scholar]
  3. Centerwall W. R., Morris J. P. Partial D 15 trisomy. A case and general review. Hum Hered. 1975;25(6):442–452. doi: 10.1159/000152759. [DOI] [PubMed] [Google Scholar]
  4. Cohen M. M., Ornoy A., Rosenmann A., Kohn G. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Ann Genet. 1975 Jun;18(2):99–103. [PubMed] [Google Scholar]
  5. Coldwell S., Fitzgerald B., Semmens J. M., Ede R., Bateman C. A case of trisomy of chromosome 15. J Med Genet. 1981 Apr;18(2):146–148. doi: 10.1136/jmg.18.2.146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Crandall B. F., Muller H. M., Bass H. N. Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding. Am J Ment Defic. 1973 Mar;77(5):571–578. [PubMed] [Google Scholar]
  7. Geneix A., Jaffray J. Y., Malet P., Foulon E., Jalbert P., Crost P. A new case of partial trisomy 15q-. Hum Genet. 1979 Oct 2;51(3):335–338. doi: 10.1007/BF00283405. [DOI] [PubMed] [Google Scholar]
  8. Magenis R. E., Overton K. M., Reiss J. A., Macfarlane J. P., Hecht F. Partial trisomy 15. Lancet. 1972 Dec 23;2(7791):1365–1366. doi: 10.1016/s0140-6736(72)92806-1. [DOI] [PubMed] [Google Scholar]
  9. McKusick V. A. The human gene map 1 December 1984. Clin Genet. 1985 Feb;27(2):207–239. doi: 10.1111/j.1399-0004.1985.tb00214.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Pfeiffer R. A., Kessel E. Partial trisomy 15q1. Hum Genet. 1976 Jul 7;33(1):77–83. doi: 10.1007/BF00447290. [DOI] [PubMed] [Google Scholar]
  11. Power M. M., Barry R. G., Cannon D. E., Masterson J. G. Familial partial trisomy 15. Ann Genet. 1977 Sep;20(3):159–165. [PubMed] [Google Scholar]
  12. Rethoré M. O., Dutrillaux B. Translocation 46,XX, t(15; 21) (q13; q22,1) chez la mère de deux enfants atteints de trisomie 15 et de monosomie 21 partielles. Ann Genet. 1973 Dec;16(4):271–275. [PubMed] [Google Scholar]
  13. Schreck R. R., Breg W. R., Erlanger B. F., Miller O. J. Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15. Hum Genet. 1977 Apr 7;36(1):1–12. doi: 10.1007/BF00390430. [DOI] [PubMed] [Google Scholar]
  14. Schweizer D., Ambros P., Andrle M. Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A. Exp Cell Res. 1978 Feb;111(2):327–332. doi: 10.1016/0014-4827(78)90177-5. [DOI] [PubMed] [Google Scholar]
  15. Taysi K., Devivo D. C., Sekhon G. S. Partial trisomy 15 and intractable seizures. Acta Paediatr Scand. 1979 May;68(3):445–447. doi: 10.1111/j.1651-2227.1979.tb05036.x. [DOI] [PubMed] [Google Scholar]
  16. Uldall P. R., Feest T. G., Morley A. R., Tomlinson B. E., Kerr D. N. Cyclophosphamide therapy in adults with minimal-change nephrotic syndrome. Lancet. 1972 Jun 10;1(7763):1250–1253. doi: 10.1016/s0140-6736(72)90978-6. [DOI] [PubMed] [Google Scholar]
  17. Wang H., Hunter A. G. A supernumerary "G" like chromosome originating from a maternal 13;15 translocation in a nondysmorphic, retarded girl. Clin Genet. 1979 Mar;15(3):273–277. doi: 10.1111/j.1399-0004.1979.tb00979.x. [DOI] [PubMed] [Google Scholar]
  18. Watson E. J., Gordon R. R. A case of partial trisomy 15. J Med Genet. 1974 Dec;11(4):400–402. doi: 10.1136/jmg.11.4.400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wisniewski L., Hassold T., Heffelfinger J., Higgins J. V. Cytogenetic and clinical studies in five cases of inv dup(15). Hum Genet. 1979 Sep;50(3):259–270. doi: 10.1007/BF00399391. [DOI] [PubMed] [Google Scholar]

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